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4-(2-Methyl-1,3-thiazol-4-yl)benzoic acid is a chemical compound characterized by its molecular formula C11H9NO2S. It is a white to off-white crystalline powder that features a thiazole ring and a benzoic acid group. 4-(2-METHYL-1,3-THIAZOL-4-YL)BENZOIC ACID is widely recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structural attributes and properties render it a valuable building block in organic synthesis, making it suitable for drug discovery and development. Additionally, it serves as a reagent in chemical research and analysis. While generally stable under normal conditions, it is essential to handle and store this chemical with standard safety measures.

294620-60-3

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294620-60-3 Usage

Uses

Used in Pharmaceutical Industry:
4-(2-METHYL-1,3-THIAZOL-4-YL)BENZOIC ACID is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(2-METHYL-1,3-THIAZOL-4-YL)BENZOIC ACID is utilized as an intermediate in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Organic Synthesis:
4-(2-METHYL-1,3-THIAZOL-4-YL)BENZOIC ACID is employed as a building block in organic synthesis, leveraging its structural features to facilitate the creation of complex organic molecules for a range of applications.
Used in Chemical Research and Analysis:
As a reagent, 4-(2-METHYL-1,3-THIAZOL-4-YL)BENZOIC ACID is used in chemical research and analysis to support the investigation of various chemical properties and reactions, contributing to the advancement of scientific knowledge in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 294620-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,6,2 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 294620-60:
(8*2)+(7*9)+(6*4)+(5*6)+(4*2)+(3*0)+(2*6)+(1*0)=153
153 % 10 = 3
So 294620-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2S/c1-7-12-10(6-15-7)8-2-4-9(5-3-8)11(13)14/h2-6H,1H3,(H,13,14)

294620-60-3SDS

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-METHYL-1,3-THIAZOL-4-YL)BENZOIC ACID

1.2 Other means of identification

Product number -
Other names 4-(2-Methyl-thiazol-4-yl)-benzoic acid

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:294620-60-3 SDS

294620-60-3Relevant academic research and scientific papers

Uncovering an allosteric mode of action for a selective inhibitor of human bloom syndrome protein

Chen, Xiangrong,Ali, Yusuf I.,Fisher, Charlotte EL,Arribas-Bosacoma, Raquel,Rajasekaran, Mohan B.,Williams, Gareth,Walker, Sarah,Booth, Jessica R.,Hudson, Jessica JR,Mark Roe,Pearl, Laurence H.,Ward, Simon E.,Pearl, Frances MG,Oliver, Antony W.

, (2021/04/02)

BLM (Bloom syndrome protein) is a RECQ-family helicase involved in the dissolution of complex DNA structures and repair intermediates. Synthetic lethality analysis implicates BLM as a promising target in a range of cancers with defects in the DNA damage r

Synthesis of heteroaromatic carboxylic acids by carbonylation of hetaryl halides with catalysts based on cobalt carbonyl modified with epoxides

Boyarskii,Zhesko,Larionov,Polukeev

, p. 571 - 575 (2008/02/14)

A new method for the synthesis of heteroaromatic acids and their derivatives (esters and salts) by carbonylation of the corresponding halides was developed. Hetaryl halides were activated in alcoholic-alkali medium by highly active catalytic systems based on cobalt carbonyl modified with epoxides, developed previously for carbonylation of aryl halides.

Benzamide nitriles

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Page 35-36, (2010/02/09)

Compounds of the formula (I) wherein m, n, A, R1, R2, R3, R4, R5 and R6 are as described herein, together with methods for making the compounds and using the compounds for treatment of diseases or conditions mediated by Cathepsin K.

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