Recently I am researching about BENZOXAZINE MONOMERS; OPENING POLYMERIZATION; COPOLYMERIZATION, Saw an article supported by the MINECO/FEDER [CTQ2015-65439-R, 2016-81797-REDC]; Generalitat de CatalunyaGeneralitat de Catalunya [2017 SGR00465]; MAPEX Center for Materials and Processes. Name: m-Methoxyphenol. Published in MDPI in BASEL ,Authors: Martos, A; Soto, M; Schafer, H; Koschek, K; Marquet, J; Sebastian, RM. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol
It is possible to control the crosslink density of polymers derived from monobenzoxazines by switching the type of substituents in the phenolic ring and their relative position with respect to the phenol group. We prepared several substituted monobenzoxazines in the para and meta positions of the phenolic ring and studied how these substituents affected the polymerization temperature of monomers and the thermal stability of the final polymers and, more extensively, how they affected the crosslink network of the final polymers. Gel content and dynamic mechanical analysis confirm that ortho- and para-orienting substituents in the meta position generate highly crosslinked materials compared to para ones. This fact can lead to the design of materials with highly crosslinked networks based on monobenzoxazines, simpler and more versatile monomers than the commercial bisbenzoxazines currently in use.
Name: m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Martos, A; Soto, M; Schafer, H; Koschek, K; Marquet, J; Sebastian, RM 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