339018-41-6

Basic information

• Product Name: 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde
• Synonyms: 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde;4-[(2-Chloro-1,3-thiazol-5-yl)methoxy]-3-methoxybenzaldehyde
• CAS NO: 339018-41-6
• Molecular Formula: C₁₂H₁₀ClNO₃S
• Molecular Weight: 283.7307
• Mol File: 339018-41-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 122～125℃
• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde(339018-41-6)
• EPA Substance Registry System: 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde(339018-41-6)

Safety Data

• Hazardous Substances Data: 339018-41-6(Hazardous Substances Data)

Usage

General Description

4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde is a chemical compound with a complex structure. It contains a 2-chlorothiazol-5-yl group, a methoxy group, and a benzaldehyde group. It is used in pharmaceutical research and drug development due to its potential medicinal properties. The 2-chlorothiazol-5-yl group gives the compound its distinctive chemical properties, while the methoxy and benzaldehyde groups contribute to its aromatic nature. 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde may have potential applications in the development of new drugs for various medical conditions.

Upstream product

• 121-33-5 vanillin 
• 105827-91-6 α-Cl-β-thiazolyl chloride 

Downstream Products

• 1234623-96-1 3-methoxy-4-((2-chlorothiazol-5-yl)methoxy)benzyl alcohol 

Relevant articles and documents

Novel vanillin derivatives containing a 1,3,4-thiadiazole moiety as potential antibacterial agents

In this study, thirty-four novel vanillin derivatives containing a 1,3,4-thiadiazole structure were obtained and their antibacterial activities were evaluated. The results indicate that most of the title compounds displayed inhibitory effects on Xanthomonas oryzae pv. oryzae (Xoo) and Xanthomonas oryzae pv. oryzicola (Xoc). Among them, compound 29 exhibited excellent antibacterial activities against Xoo and Xoc in vitro, with the EC50 values of 3.14 and 8.83 μg/mL, respectively, much superior to thiodiazole copper (87.03 and 108.99 μg/mL) and bismerthiazol (67.64 and 79.26 μg/mL). Under greenhouse condition, the protective efficiency of compound 29 against rice bacterial leaf blight was 49.34%, and curative efficiency was 40.96%. In addition, compound 29 can reduce the exopolysaccharides production of Xoo, increase the permeability of cell membrane and damage cell membrane.