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2-Thiazolamine, 5-chloro-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50729-62-9

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50729-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50729-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50729-62:
(7*5)+(6*0)+(5*7)+(4*2)+(3*9)+(2*6)+(1*2)=119
119 % 10 = 9
So 50729-62-9 is a valid CAS Registry Number.

50729-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-4-phenyl-1,3-thiazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-4-Phenyl-5-chlorthiazol

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:50729-62-9 SDS

50729-62-9Relevant academic research and scientific papers

Site-Selective Thiolation of (Multi)halogenated Heteroarenes

Sandfort, Frederik,Knecht, Tobias,Pinkert, Tobias,Daniliuc, Constantin G.,Glorius, Frank

supporting information, p. 6913 - 6919 (2020/05/14)

A general and simple strategy for the site-selective thiolation of various pharmaceutically relevant electron-rich heteroarenes with thiols is reported. This mild and reliable photocatalytic protocol enables C-S coupling at the most electron-rich position of the (multi)halogenated substrates, complementing established methodologies. Experimental and computational studies suggest a radical chain mechanism with the key step being a homolytic aromatic substitution of the heteroaryl halide by an electrophilic thiyl radical, highlighting an underdeveloped reactivity mode.

SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF NUCLEASES

-

Page/Page column 14; 57-58, (2019/11/12)

The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3, R4, R5, R6 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.

THIAZOLE MODULATORS OF A3 ADENOSINE RECEPTORS

-

Paragraph 0147, (2017/12/27)

Modulators of adenosin A3 receptors of formula (I) and procedure for preparing these compounds. Other objectives of the present invention are to provide pharmaceutical compositions comprising an effective amount of these compounds and the use o

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