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4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde is a complex chemical compound that features a 2-chlorothiazol-5-yl group, a methoxy group, and a benzaldehyde group. This unique combination of functional groups endows the compound with distinctive chemical properties and an aromatic character, making it a promising candidate for pharmaceutical research and drug development.

339018-41-6

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339018-41-6 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde is utilized as a key intermediate in the synthesis of new drugs, given its potential medicinal properties. 4-((2-Chlorothiazol-5-yl)Methoxy)-3-Methoxybenzaldehyde's distinctive chemical features, including the 2-chlorothiazol-5-yl group, contribute to its versatility in the development of pharmaceutical agents for various medical conditions. Its aromatic nature, due to the presence of methoxy and benzaldehyde groups, further enhances its applicability in creating novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 339018-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,0,1 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 339018-41:
(8*3)+(7*3)+(6*9)+(5*0)+(4*1)+(3*8)+(2*4)+(1*1)=136
136 % 10 = 6
So 339018-41-6 is a valid CAS Registry Number.

339018-41-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2-chloro-1,3-thiazol-5-yl)methoxy]-3-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-methoxy-4-((2-chlorothiazol-5-yl)methoxy)benzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:339018-41-6 SDS

339018-41-6Relevant academic research and scientific papers

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

Cai, Hui,Gan, Xiuhai,Li, Shaoyuan,Song, Baoan,Wu, Qiong,Yuan, Ting

supporting information, (2020/03/24)

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.

Synthesis and herbicidal activities of 2-cyano-3-benzylaminoacrylates containing thiazole moiety

Wang, Tingting,Bing, Guifang,Zhang, Xin,Qin, Zhenfang,Yu, Haibo,Qin, Xue,Dai, Hong,Miao, Wenke,Wu, Shanshan,Fang, Jianxin

supporting information; experimental part, p. 3348 - 3351 (2010/07/16)

Two series of novel 2-cyano-3-benzylaminoacrylates containing long-chain thiazole ring moiety were synthesized as herbicidal inhibitors of photosystem II (PS II) electron transportation. Their structures were confirmed by 1H NMR and elemental a

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