914348-82-6

Usage

Uses

Used in Pharmaceutical Industry:
2-(4-Methoxyphenyl)thiazole-5-carbaldehyde is used as a building block for the synthesis of biologically active compounds. Its unique structure allows for the creation of pharmaceuticals with potential therapeutic applications, contributing to the development of new drugs and treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-Methoxyphenyl)thiazole-5-carbaldehyde serves as a key intermediate in the production of agrochemicals, such as pesticides and herbicides. Its reactivity and structural properties enable the synthesis of compounds with specific pesticidal or herbicidal activities, enhancing crop protection and yield.
Used in Research Laboratories:
2-(4-Methoxyphenyl)thiazole-5-carbaldehyde is utilized in research settings for organic synthesis and chemical analysis. Its versatility as a chemical intermediate facilitates the exploration of new synthetic pathways and the development of novel compounds with potential applications in various fields.

InChI:InChI=1/C11H9NO2S/c1-14-9-4-2-8(3-5-9)11-12-6-10(7-13)15-11/h2-7H,1H3

Upstream product

• 464192-28-7 2-bromo-1,3-thiazole-5-carbaldehyde 
• 5720-07-0 4-methoxyphenylboronic acid 
• 27088-84-2 2-(4-methoxyphenyl)-1,3-thiazole 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 937668-37-6 5-Hydroxymethyl-2-(4-methoxyphenyl)-thiazole 
• 1204423-52-8 5-Bromomethyl-2-(4-methoxyphenyl)-thiazole 
• 1204423-53-9 3-[2-(4-Methoxyphenyl)thiazol-5-yl]-2-fluoropropionic acid 
• 1204423-56-2 4-{3-[2-(4-Methoxyphenyl)thiazol-5-yl]-2-fluoropropanoyl}amino-1-ethylpyrrole-3-carboxylic acid 
• 1204424-02-1 3-[2-(4-Methoxyphenyl)thiazol-5-yl]-2,2-difluoropropionic acid 
• 1204423-54-0 C₁₈H₂₀FNO₅S 
• 1204423-57-3 C₂₃H₂₄FN₃O₄S 
• 1204424-03-2 C₁₅H₁₅F₂NO₃S 
• 27088-84-2 2-(4-methoxyphenyl)-1,3-thiazole 

Relevant academic research and scientific papers

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.

NITROGEN-CONTAINING AROMATIC HETEROCYCLYL COMPOUND

The present invention provides a compound having excellent regulating action on blood lipid level. The present invention provides a compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof, etc., wherein A represents a 5-membered nitrogen-containing aromatic heterocyclyl group; R1 represents COOH or the like; each R2 represents an alkyl or the like; each R3 represents an optionally substituted phenyl, an optionally substituted phenylalkyl, or the like; m represents 0, 1, 2, or 3; n represents 0 or 1; each of R4, R5, R6, and R7 represents H, an alkyl, or the like; and B represents an optionally substituted naphthyl, an optionally substituted aromatic heterocyclyl, or a group represented by the following formula (II) wherein each of B1 and B2 represents an optionally substituted phenyl or an optionally substituted aromatic heterocyclyl.