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5-Thiazolecarboxaldehyde, 4-methyl-2-(3-methylphenyl)- is a chemical compound with the molecular formula C11H9NOS. It is a derivative of thiazolecarboxaldehyde, featuring a methyl group at the 4-position and a 3-methylphenyl group at the 2-position. 5-Thiazolecarboxaldehyde, 4-methyl-2-(3-methylphenyl)- is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is known for its unique chemical properties, such as its reactivity towards nucleophiles and its ability to form stable adducts. The compound is typically synthesized through various chemical reactions, including condensation and cyclization processes. Due to its potential applications in the development of new drugs and other chemical products, research on 5-Thiazolecarboxaldehyde, 4-methyl-2-(3-methylphenyl)- and its derivatives continues to be an active area of study in the field of organic chemistry.

61292-02-2

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61292-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61292-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,9 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61292-02:
(7*6)+(6*1)+(5*2)+(4*9)+(3*2)+(2*0)+(1*2)=102
102 % 10 = 2
So 61292-02-2 is a valid CAS Registry Number.

61292-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-(3-methylphenyl)-1,3-thiazole-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-methyl-2-m-tolyl-thiazole-5-carbaldehyde

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:61292-02-2 SDS

61292-02-2Downstream Products

61292-02-2Relevant academic research and scientific papers

Synthesis and antimycobacterial evaluation of new 5-(1-benzyl-1H-1,2,3-triazol-4-yl)-4-methyl-2-arylthiazole derivatives

Shinde, Vikas,Mahulikar, Pramod,Mhaske, Pravin C.,Chakraborty, Shakti,Choudhari, Amit,Phalle, Siddharth,Choudhari, Prafulla,Sarkar, Dhiman

, p. 805 - 819 (2019/04/26)

A new series of 5-(1-benzyl-1H-1,2,3-triazol-4-yl)-4-methyl-2-arylthiazole derivatives, 6a?w have been synthesized by click reaction of substituted benzylazide, 5a?d with 5-ethynyl-4-methyl-2-substituted phenylthiazole, 4a?f. The starting compounds 4-ethy

Synthesis, antimycobacterial screening and molecular docking studies of 4-aryl-4′-methyl-2′-aryl-2,5′-bisthiazole derivatives

Abhale, Yogita K.,Shinde, Abhijit D.,Deshmukh, Keshav K.,Nawale, Laxman,Sarkar, Dhiman,Choudhari, Prafulla B.,Kumbhar, Santosh S.,Mhaske, Pravin C.

, p. 2889 - 2899 (2017/10/06)

A series of 4-aryl-4′-methyl-2′-aryl-2,5′-bisthiazole derivatives (5a–o) were synthesized and screened for inhibitory activity against Mycobacterium tuberculosis H37Ra (ATCC 25177) and Mycobacterium bovis BCG (ATCC 35743) strains. Five lead compounds (5e,

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