1404493-66-8

Basic information

• Product Name: 2-(4-chlorobenzyl)-4-methylthiazole-5-carbaldehyde
• Synonyms: 2-(4-chlorobenzyl)-4-methylthiazole-5-carbaldehyde
• CAS NO: 1404493-66-8
• Molecular Weight: 251.737
• Mol File: 1404493-66-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(4-chlorobenzyl)-4-methylthiazole-5-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-chlorobenzyl)-4-methylthiazole-5-carbaldehyde(1404493-66-8)
• EPA Substance Registry System: 2-(4-chlorobenzyl)-4-methylthiazole-5-carbaldehyde(1404493-66-8)

Safety Data

• Hazardous Substances Data: 1404493-66-8(Hazardous Substances Data)

Upstream product

• 1267019-59-9 (2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methanol 
• 1200399-45-6 ethyl 2-[(4-chlorophenyl)methyl]-4-methyl-1,3-thiazole-5-carboxylate 

Downstream Products

• 1453840-25-9 1-((2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methyleneamino)-2-ethylisothiourea 
• 1453840-29-3 1-((2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methyleneamino)-2-propylisothiourea 
• 1453840-33-9 1-((2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methyleneamino)-2-isopropylisothiourea 
• 1453840-21-5 1-((2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methylene) thiosemicarbazide 
• 1649449-19-3 N-((2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methylene)-4-(2-(4-chlorophenyl)thiazol-4-yl)benzenamine 
• 1649449-28-4 2-(2-(4-chlorobenzyl)-4-methylthiazol-5-yl)-3-(4-(2-(4-chlorophenyl)thiazol-4-yl)phenyl)thiazolidin-4-one 
• 1649449-18-2 N-((2-(4-chlorobenzyl)-4-methylthiazol-5-yl)methylene)-4-(2-methylthiazol-4-yl)benzenamine 
• 1649449-27-3 2-(2-(4-chlorobenzyl)-4-methylthiazol-5-yl)-3-(4-(2-methylthiazol-4-yl)phenyl)thiazolidin-4-one 

Relevant articles and documents

Synthesis and antimicrobial activities of novel series of 3-(4-(2-substituted thiazol-4-yl)phenyl)-2-(4-methyl-2-substituted thiazol-5-yl)thiazolidin-4-one derivatives

In the present investigation, a novel series of 3-(4-(2-substituted thiazol-4-yl)phenyl)-2-(4-methyl-2-substituted thiazol-5-yl)thiazolidin-4-one derivatives were synthesized by condensation of 2-substituted-4-methylthiazole- 5-carbaldehyde with 4-(2-subs