What about chemistry interests you the most 120-14-9

Category: indole-building-block. Welcome to talk about 120-14-9, If you have any questions, you can contact Wang, P; Zhang, BZ or send Email.

An article Sustainable aromatic polyesters with 1,5-disubstituted indole units WOS:000649534900037 published article about TEREPHTHALATE POLYESTERS; CATALYTIC CONVERSION; THERMAL-PROPERTIES; BUILDING-BLOCKS; BIFURAN DIESTER; VANILLIC ACID; DEGRADATION; CRYSTALLIZATION; COPOLYESTERS; BIOPOLYMER in [Wang, Ping; Zhang, Baozhong] Lund Univ, Ctr Anal & Synth, POB 124, SE-22100 Lund, Sweden in 2021.0, Cited 76.0. Category: indole-building-block. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9

This work aims to unravel the impact of disubstitution patterns on the physical properties and processing characteristics of indole-based aromatic polyesters. A series of hydroxyl-carboxylate (AB-type) monomers with 1,5-disubstituted indole and 3-6 methylene units was conveniently synthesized and used in bulk polycondensation to yield the corresponding polyesters with decent molecular weight. These new monomers and polyesters showed enhanced thermal stability compared to the previously reported monomers and polyesters with a 1,3-disubstituted indole structure. According to DSC results, these polyesters showed tunable glass transition temperatures (T-g similar to 57-80 degrees C), depending on the length of the aliphatic methylene units. DSC and WAXD measurements revealed that these polymers did not crystalize from melt, but the ones with 3 or 5 methylene units per repeating unit crystalized from solution. Finally, we demonstrated that the new polyesters with 1,5-disubstituted indole units could be crosslinked using sustainable aromatic aldehyde, which could further enhance their thermal properties.

Category: indole-building-block. Welcome to talk about 120-14-9, If you have any questions, you can contact Wang, P; Zhang, BZ or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Chemical Properties and Facts of 100-83-4

Welcome to talk about 100-83-4, If you have any questions, you can contact Abdella, AM; Abdelmoniem, AM; Butenschon, H; Abdelhamid, IA; Elwahy, AHM or send Email.. Formula: C7H6O2

Formula: C7H6O2. Recently I am researching about MULTICOMPONENT REACTIONS; KNOEVENAGEL CONDENSATION; FUSED HETEROCYCLES; ANTITUMOR-ACTIVITY; DERIVATIVES; BEARING; DESIGN; PYRANO; GREEN; POT, Saw an article supported by the Alexander von Humboldt FoundationAlexander von Humboldt Foundation. Published in ARKAT USA INC in GAINESVILLE ,Authors: Abdella, AM; Abdelmoniem, AM; Butenschon, H; Abdelhamid, IA; Elwahy, AHM. The CAS is 100-83-4. Through research, I have a further understanding and discovery of 3-Hydroxybenzaldehyde

A synthesis of novel bis(1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitriles), bis(4H-chromene-3-carbonitriles) and bis(dihydropyrano[3,2-c]chromenes), which are linked to aliphatic spacers via amide linkages was achieved via multicomponent reactions (MCR) of the appropriate bis-aldehyde with two equivalents of both of malononitrile and 3-methylpyrazol-5-one, dimedone or 4-hydroxycoumarin in a basic solution. [GRAPHICS] .

Welcome to talk about 100-83-4, If you have any questions, you can contact Abdella, AM; Abdelmoniem, AM; Butenschon, H; Abdelhamid, IA; Elwahy, AHM or send Email.. Formula: C7H6O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Extended knowledge of C7H8O2

COA of Formula: C7H8O2. Welcome to talk about 150-19-6, If you have any questions, you can contact Sniecikowska, J; Gluch-Lutwin, M; Bucki, A; Wieckowska, A; Siwek, A; Jastrzebska-Wiesek, M; Partyka, A; Wilczynska, D; Pytka, K; Latacz, G; Przejczowska-Pomierny, K; Wyska, E; Wesolowska, A; Pawlowski, M; Newman-Tancredi, A; Kolaczkowski, M or send Email.

Recently I am researching about FUNCTIONAL SELECTIVITY; DRUG DISCOVERY; SEROTONIN; ANTAGONIST; METABOLISM; AGENTS; POTENT; RATS; HIPPOCAMPUS; ANXIOLYTICS, Saw an article supported by the National Science Centre (NCN)National Science Centre, Poland [2015/19/B/NZ7/03543]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Sniecikowska, J; Gluch-Lutwin, M; Bucki, A; Wieckowska, A; Siwek, A; Jastrzebska-Wiesek, M; Partyka, A; Wilczynska, D; Pytka, K; Latacz, G; Przejczowska-Pomierny, K; Wyska, E; Wesolowska, A; Pawlowski, M; Newman-Tancredi, A; Kolaczkowski, M. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol. COA of Formula: C7H8O2

Novel 1-(1-benzoylpiperidin-4-yl)methanamine derivatives with high affinity and selectivity for serotonin 5-HT1A receptors were obtained and tested in four functional assays: ERK1/2 phosphorylation, adenylyl cyclase inhibition, calcium mobilization, and beta-arrestin recruitment. Compounds 44 and 56 (2-methylaminophenoxyethyl and 2-(1H-indol-4-yloxy)ethyl derivatives, respectively) were selected as biased agonists with highly differential signaling fingerprints that translated into distinct in vivo profiles. In vitro, 44 showed biased agonism for ERK1/2 phosphorylation and, in vivo, it preferentially exerted an antidepressant-like effect in the Porsolt forced swimming test in rats. In contrast, compound 56 exhibited a first-in-class profile: it preferentially and potently activated beta-arrestin recruitment in vitro and potently elicited lower lip retraction in vivo, a component of serotonergic syndrome. Both compounds showed promising developability properties. The presented 5-HT1A receptor-biased agonists, preferentially targeting various signaling pathways, have the potential to become drug candidates for distinct central nervous system pathologies and possessing accentuated therapeutic activity and reduced side effects.

COA of Formula: C7H8O2. Welcome to talk about 150-19-6, If you have any questions, you can contact Sniecikowska, J; Gluch-Lutwin, M; Bucki, A; Wieckowska, A; Siwek, A; Jastrzebska-Wiesek, M; Partyka, A; Wilczynska, D; Pytka, K; Latacz, G; Przejczowska-Pomierny, K; Wyska, E; Wesolowska, A; Pawlowski, M; Newman-Tancredi, A; Kolaczkowski, M or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

The Best Chemistry compound:C5H8O2

Bye, fridends, I hope you can learn more about C5H8O2, If you have any questions, you can browse other blog as well. See you lster.. Safety of (E)-2-Methylbut-2-enoic acid

Safety of (E)-2-Methylbut-2-enoic acid. Chen, Z; Liu, F; Liu, NN in [Chen, Zhou; Liu, Feng; Liu, Nannan] Auburn Univ, Dept Entomol & Plant Pathol, Auburn, AL 36849 USA published Human Odour Coding in the Yellow Fever Mosquito, Aedes aegypti in 2019, Cited 45. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1.

Insects use their olfactory systems to obtain chemical information on mating partners, oviposition sites and food. The yellow fever mosquito Aedes aegypti, an important vector of human infectious diseases, shows strong preference for human blood meals. This study investigated the chemical basis of host detection by characterizing the neuronal responses of antenna! olfactory sensilla of female Ae. aegypti to 103 compounds from human skin emanations. The effect of blood feeding on the responses of olfactory sensilla to these odorants was examined as well. Sensilla SBTII, GP, and three functional subtypes of SST (SST1, SST2, and SST3) responded to most of the compounds tested. Olfactory receptor neurons (ORNs) ‘A’ and ‘B’ in the trichoid sensilla, either activated or inhibited, were involved in the odour coding process. Compounds from different chemical classes elicited responses with different temporal structures and different response patterns across the olfactory sensilla. Except for their increased responses to several odorants, blood-fed mosquitoes generally evoked reduced responses to specific aldehydes, alcohols, aliphatics/aromatics, ketones, and amines through the SST1, SST2, SBTI, SBTII and GP sensilla. The odorants eliciting diminished responses in female mosquitoes after blood feeding may be important in Ae. aegypti host-seeking activity and thus can be candidates for mosquito attractants in the process of this disease vector management.

Bye, fridends, I hope you can learn more about C5H8O2, If you have any questions, you can browse other blog as well. See you lster.. Safety of (E)-2-Methylbut-2-enoic acid

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Chemical Properties and Facts of 99-93-4

Safety of 4′-Hydroxyacetophenone. Welcome to talk about 99-93-4, If you have any questions, you can contact Xu, YT; Li, CY; Huang, XB; Gao, WX; Zhou, YB; Liu, MC; Wu, HY or send Email.

In 2019 GREEN CHEM published article about AEROBIC OXIDATIVE HYDROXYLATION; HIGHLY EFFICIENT CONVERSION; ARYL BORONIC ACIDS; IPSO-HYDROXYLATION; VISIBLE-LIGHT; CATALYZED HYDROXYLATION; PHOTOREDOX CATALYSIS; PHENOLS; MILD; GENERATION in [Xu, Yu-Ting; Li, Chen-Yuan; Huang, Xiao-Bo; Gao, Wen-Xia; Zhou, Yun-Bing; Liu, Miao-Chang; Wu, Hua-Yue] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China in 2019, Cited 46. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Safety of 4′-Hydroxyacetophenone

Photoinduced hydroxylation of boronic acids with molecular oxygen under photocatalyst-free conditions is reported, providing a green entry to a variety of phenols and aliphatic alcohols in a highly concise fashion. This new protocol features photocatalyst-free conditions, wide substrate scope and excellent functional group compatibility.

Safety of 4′-Hydroxyacetophenone. Welcome to talk about 99-93-4, If you have any questions, you can contact Xu, YT; Li, CY; Huang, XB; Gao, WX; Zhou, YB; Liu, MC; Wu, HY or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Interesting scientific research on C8H8O2

Formula: C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Podunavac, M; Mailyan, AK; Jackson, JJ; Lovy, A; Farias, P; Huerta, H; Molgo, J; Cardenas, C; Zakarian, A or concate me.

Formula: C8H8O2. Authors Podunavac, M; Mailyan, AK; Jackson, JJ; Lovy, A; Farias, P; Huerta, H; Molgo, J; Cardenas, C; Zakarian, A in WILEY-V C H VERLAG GMBH published article about in [Podunavac, Masa; Mailyan, Artur K.; Jackson, Jeffrey J.; Cardenas, Cesar; Zakarian, Armen] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA; [Lovy, Alenka; Farias, Paula; Huerta, Hernan; Cardenas, Cesar] Univ Mayor, Ctr Integrat Biol, Fac Sci, Gerosci Ctr Brain Hlth & Metab, Santiago, Chile; [Molgo, Jordi] Univ Paris Saclay, CEA, Inst Sci Vivant Frederic Joliot,Serv Ingn Mol San, ERL CNRS N 9004,Dept Medicaments & Technol Sante, Batiment 152,Point Courrier 24, F-91191 Gif Sur Yvette, France; [Cardenas, Cesar] Buck Inst Res Aging, Novato, CA 94945 USA in 2021.0, Cited 33.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

The scalable synthesis of the oxaquinolizidine marine natural product desmethylxestospongin B is based on the early application of Ireland-Claisen rearrangement, macrolactamization, and a late-stage installation of the oxaquinolizidine units by lactam reduction. The synthesis serves as the source of material to investigate calcium signaling and its effect on mitochondrial metabolism in various cell types, including cancer cells.

Formula: C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Podunavac, M; Mailyan, AK; Jackson, JJ; Lovy, A; Farias, P; Huerta, H; Molgo, J; Cardenas, C; Zakarian, A or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Awesome and Easy Science Experiments about C8H8O2

Welcome to talk about 99-93-4, If you have any questions, you can contact Eltoukhy, A; Jia, Y; Nahurira, R; Abo-Kadoum, MA; Khokhar, I; Wang, JH; Yan, YC or send Email.. Application In Synthesis of 4′-Hydroxyacetophenone

Application In Synthesis of 4′-Hydroxyacetophenone. Eltoukhy, A; Jia, Y; Nahurira, R; Abo-Kadoum, MA; Khokhar, I; Wang, JH; Yan, YC in [Eltoukhy, Adel; Jia, Yang; Nahurira, Ruth; Khokhar, Ibatsam; Wang, Junhuan; Yan, Yanchun] Chinese Acad Agr Sci, Grad Sch, Beijing 100081, Peoples R China; [Eltoukhy, Adel; Abo-Kadoum, M. A.] Al Azhar Univ, Dept Bot & Microbiol, Fac Sci, Assiut 71524, Egypt; [Abo-Kadoum, M. A.] Southwest Univ, Inst Modern Biopharmaceut, Sch Life Sci, Chongqing 400715, Peoples R China published Biodegradation of endocrine disruptor Bisphenol A by Pseudomonas putida strain YC-AE1 isolated from polluted soil, Guangdong, China in 2020.0, Cited 55.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

Background Bisphenol A is an important organic chemical as an intermediate, final and inert ingredient in manufacturing of many important products like polycarbonate plastics, epoxy resins, flame retardants, food-drink packaging coating, and other. BPA is an endocrine disruptor compound that mimics the function of estrogen causing damage to reproductive organs. Bacterial degradation has been consider as a cost effective and eco-friendly method for BPA degradation compared with physical and chemical methods. This study aimed to isolate and identify bacterial strain capable to degrade and tolerate high concentrations of this pollutant, studying the factors affecting the degradation process and study the degradation mechanism of this strain. Results YC-AE1 is a Gram negative bacterial strain isolated from soil and identified as Pseudomonas putida by 16S rRNA gene sequence and BIOLOG identification system. This strain found to have a high capacity to degrade the endocrine disruptor Bisphenol A (BPA). Response surface methodology using central composite design was used to statistically optimize the environmental factors during BPA degradation and the results obtained by significant model were 7.2, 30 degrees C and 2.5% for optimum initial pH, temperature and inoculum size, respectively. Prolonged incubation period with low NaCl concentration improve the biodegradation of BPA. Analysis of variance (ANOVA) showed high coefficient of determination, R-2 and Adj-R-2 which were 0.9979 and 0.9935, respectively. Substrate analysis found that, strain YC-AE1 could degrade a wide variety of bisphenol A-related pollutants such as bisphenol B, bisphenol F, bisphenol S, Dibutyl phthalate, Diethylhexyl phthalate and Diethyl phthalate in varying proportion. Pseudomonas putida YC-AE1 showed high ability to degrade a wide range of BPA concentrations (0.5-1000 mg l(- 1)) with completely degradation for 500 mg l(- 1) within 72 h. Metabolic intermediates detected in this study by HPLC-MS were identified as 4,4-dihydroxy-alpha-methylstilbene, p-hydroxybenzaldeyde, p-hydroxyacetophenone, 4-hydroxyphenylacetate, 4-hydroxyphenacyl alcohol, 2,2-bis(4-hydroxyphenyl)-1-propanol, 1,2-bis(4-hydroxyphenyl)-2-propanol and 2,2-bis(4-hydroxyphenyl) propanoate. Conclusions This study reports Pseudomonas putida YC-AE1 as BPA biodegrader with high performance in degradation and tolerance to high BPA concentration. It exhibited strong degradation capacity and prominent adaptability towards a wide range of environmental conditions. Moreover, it degrades BPA in a short time via two different degradation pathways.

Welcome to talk about 99-93-4, If you have any questions, you can contact Eltoukhy, A; Jia, Y; Nahurira, R; Abo-Kadoum, MA; Khokhar, I; Wang, JH; Yan, YC or send Email.. Application In Synthesis of 4′-Hydroxyacetophenone

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Extracurricular laboratory: Synthetic route of 100-83-4

Product Details of 100-83-4. Bye, fridends, I hope you can learn more about C7H6O2, If you have any questions, you can browse other blog as well. See you lster.

Product Details of 100-83-4. In 2020.0 CHEMISTRYSELECT published article about BIOLOGICAL EVALUATIONS; CHEMISTRY; EFFICIENT; HETEROCYCLES; FRAMEWORK; SOLVENT; ANALOGS; DESIGN in [Nazeef, Mohd; Tiwari, Saurabh Kumar; Yadav, Vikas; Ansari, Saif; Siddiqui, I. R.] Univ Allahabad, Lab Green Synth, Dept Chem, Allahabad 211002, Uttar Pradesh, India; [Saquib, Mohammad] Univ Allahabad, Dept Chem, Allahabad 211002, Uttar Pradesh, India; [Sagir, Hozeyfa] Paliwal PG Coll, Dept Chem, Shikohabad 283135, India; [Hussain, Mohd. Kamil] Govt Raza PG Coll, Dept Chem, Rampur 244901, India in 2020.0, Cited 46.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

A series of benzo[a]chromeno[2,3-c]phenazine derivatives were synthesized through an efficient one-pot, multicomponent eco-friendly reaction of 2-hydroxynaphthalene-1,4-dione, o-phenylenediamines, cyclic 1,3-dicarbonyl compounds and aromatic aldehydes, promoted by glycerol. To the best of our knowledge this is the first catalyst free protocol for synthesis of this important scaffold having potential applications in medicinal and materials chemistry. Other important attributes of the present method are the use of glycerol as a bio-renewable and biodegradable reaction medium-cum-promoter, use of readily available substrates, mild reaction conditions, operational simplicity, broad substrate scope, short reaction time, easy workup, and high yields and atom efficiency, which makes the disclosed protocol a superior alternative to existing methods.

Product Details of 100-83-4. Bye, fridends, I hope you can learn more about C7H6O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Let`s talk about compound :4-Hydroxyquinolin-2(1H)-one

Computed Properties of C9H7NO2. About 4-Hydroxyquinolin-2(1H)-one, If you have any questions, you can contact Aly, AA; Hassan, AA; Mohamed, NK; Abd El-Haleem, LE; Brase, S or concate me.

Computed Properties of C9H7NO2. Authors Aly, AA; Hassan, AA; Mohamed, NK; Abd El-Haleem, LE; Brase, S in SAGE PUBLICATIONS LTD published article about in [Aly, Ashraf A.; Hassan, Alaa A.; Mohamed, Nasr K.; Abd El-Haleem, Lamiaa E.] Menia Univ, Fac Sci, Chem Dept, El Minia 61519, Egypt; [Brase, Stefan] Karlsruhe Inst Technol, Inst Biol & Chem Syst Funct Mol Syst IBCS FMS, Eggenstein Leopoldshafen, Germany in 2020, Cited 13. The Name is 4-Hydroxyquinolin-2(1H)-one. Through research, I have a further understanding and discovery of 86-95-3

A novel series of 7,8-dichlorobenzofuro[3,2-c]quinoline-6,9,10(5H)-triones was obtained regioselectively in good yields. The products were formed by the reactions of the 4-hydroxy-2(1H)-quinolinones with 3,4,5,6-tetrachloro-1,2-benzoquinone in tetrahydrofuran as the solvent. Infrared, nuclear magnetic resonance (two-dimensional nuclear magnetic resonance), mass spectra and elemental analysis were used to elucidate the structures of new compounds.

Computed Properties of C9H7NO2. About 4-Hydroxyquinolin-2(1H)-one, If you have any questions, you can contact Aly, AA; Hassan, AA; Mohamed, NK; Abd El-Haleem, LE; Brase, S or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

When did you first realize you had a special interest and talent in3-(Trifluoromethyl)phenol

Bye, fridends, I hope you can learn more about C7H5F3O, If you have any questions, you can browse other blog as well. See you lster.. Computed Properties of C7H5F3O

Zhao, LX; Jiang, MJ; Hu, JJ; Zou, YL; Cheng, Y; Ren, T; Gao, S; Fu, Y; Ye, F in [Zhao, Li-Xia; Jiang, Mao-Jun; Hu, Jia-Jun; Zou, Yue-Li; Cheng, Yuan; Ren, Tao; Gao, Shuang; Fu, Ying; Ye, Fei] Northeast Agr Univ, Coll Sci, Dept Appl Chem, Harbin 150030, Peoples R China published Design, Synthesis, and Herbicidal Activity of Novel Diphenyl Ether Derivatives Containing Fast Degrading Tetrahydrophthalimide in 2020, Cited 42. Computed Properties of C7H5F3O. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9.

To seek new protoporphyrinogen oxidase (PPO) inhibitors with better biological activity, a series of novel diphenyl ether derivatives containing tetrahydrophthalimide were designed based on the principle of substructure splicing and bioisomerization. PPO inhibition experiments exhibited that 6c is the most potential compound, with the half-maximal inhibitory concentration (IC50) value of 0.00667 mg/L, showing 7 times higher activity than Oxyfluorfen (IC50 = 0.0426 mg/L) against maize PPO and similar herbicidal activities to Oxyfluorfen in weeding experiments in greenhouses and field weeding experiments. In view of the inspected bioactivities, the structure-activity relationship (SAR) of this series of compounds was also discussed. Crop selection experiments demonstrate that compound 6c is safe for soybeans, maize, rice, peanuts, and cotton at a dose of 300 g ai/ha. Accumulation analysis experiments showed that the accumulation of 6c in some crops (soybeans, peanuts, and cotton) was significantly lower than Oxyfluorfen. Current work suggests that compound 6c may be developed as a new herbicide candidate in fields.

Bye, fridends, I hope you can learn more about C7H5F3O, If you have any questions, you can browse other blog as well. See you lster.. Computed Properties of C7H5F3O

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles