Why Are Children Getting Addicted To 123-11-5

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Diab, HM; Salem, ME; Elwahy, AHM; Abdelhamid, IA or concate me.. Name: 4-Methoxybenzaldehyde

An article Bis(sulfanediyl)bis(6-aminopyrimidin-4-ones): Versatile precursors for novel bis(sulfanediyl)bis(tetrahydropyrimido[4,5-b]quinoline-4,6-diones) linked to aliphatic spacer via multi-component reactions WOS:000649632800001 published article about SUBSTITUTED MACROCYCLIC LIGANDS; POT 3-COMPONENT SYNTHESIS; SPIRO CYCLIC 2-OXINDOLE; LIGHT-EMITTING-DIODES; FUSED HETEROCYCLES; PYRIMIDINE-DERIVATIVES; BIOLOGICAL EVALUATION; DESIGN; DOCKING; AZAENAMINES in [Diab, Hadeer M.; Salem, Mostafa E.; Elwahy, Ahmed H. M.; Abdelhamid, Ismail A.] Cairo Univ, Dept Chem, Fac Sci, Giza, Egypt in 2021.0, Cited 86.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Name: 4-Methoxybenzaldehyde

A synthesis of novel bis(sulfanediyl)bis(tetrahydropyrimido[4,5-b]quinoline-4,6-diones), linked to aryl, heteroaryl, and spirocyclic-oxindole moieties at position-5, as novel hybrid molecules was reported. 2,2′-(Butane-1,4-diylbis(sulfanediyl))bis(6-aminopyrimidin-4(1H)-one) was utilized as a precursor to our target compounds via a multicomponent reaction with two equivalents of both of the appropriate aldehyde and dimedone. The target compounds were alternatively obtained by bis-(alkylation) of the appropriate 5-aryl-2-thioxohexahydropyrimido[4,5-b]quinoline-4,6-dione with 1,4-dibromobutane in moderate basic medium.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Diab, HM; Salem, ME; Elwahy, AHM; Abdelhamid, IA or concate me.. Name: 4-Methoxybenzaldehyde

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