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228413-61-4

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228413-61-4 Usage

Structural Composition

Derivative of thiazole
Contains a five-membered ring with four carbon atoms, one nitrogen atom, and one sulfur atom

Functional Groups

Carboxylic acid group: Imparts acidic properties
Amino group: Provides basic properties
Phenyl group: Part of the phenylthiazole class of compounds

Pharmaceutical Applications

Potential for antibacterial and antifungal drug development

Biological Activities

Potential for other biological activities warranting further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 228413-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,4,1 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 228413-61:
(8*2)+(7*2)+(6*8)+(5*4)+(4*1)+(3*3)+(2*6)+(1*1)=124
124 % 10 = 4
So 228413-61-4 is a valid CAS Registry Number.

228413-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-phenyl-1,3-thiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-amino-4-phenylthiazol-5-ylcarboxylic 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:228413-61-4 SDS

228413-61-4Relevant articles and documents

Solvent-Controlled Synthesis of Thiocyanated Enaminones and 2-Aminothiazoles from Enaminones, KSCN, and NBS

Chen, Xue,Cuan, Xiaodan,Duan, Xiyan,Li, Huimin,Liu, Kun,Liu, Xiaojing,Wang, Junqin,Wang, Lin,Zhou, Huiyun

, (2019/10/11)

An effective and simple solvent-controlled synthesis of thiocyanated enaminones and 2-aminothiazoles has been demonstrated from enaminones, potassium thiocyanate, and N-bromosuccinimide. This process features mild reaction conditions, simple and easy oper

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