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774-50-5

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774-50-5 Usage

General Description

2-AMINO-5-(4-FLUOROPHENYL)-THIAZOLE is a chemical compound with the molecular formula C8H6FN3S. It is a thiazole derivative that contains an amino group and a fluorine-substituted phenyl ring. 2-AMINO-5-(4-FLUOROPHENYL)-THIAZOLE is commonly used as a ligand in coordination chemistry and is also used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has been found to exhibit antimicrobial and anticancer properties, making it a potential candidate for drug development. Additionally, it is used in the manufacturing of dyes, pigments, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 774-50-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 774-50:
(5*7)+(4*7)+(3*4)+(2*5)+(1*0)=85
85 % 10 = 5
So 774-50-5 is a valid CAS Registry Number.

774-50-5SDS

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 5-(4-Fluorophenyl)-1,3-thiazol-2-amine

1.2 Other means of identification

Product number -
Other names 5-(4-fluoro-phenyl)-thiazol-2-ylamine

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:774-50-5 SDS

774-50-5Relevant articles and documents

NOVEL COMPOUNDS

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Page/Page column 101, (2016/04/20)

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C-terminal hydrolase L1 (UCHL1). The invention further relates to the use of DUB inhibitors in the treatment of cancer and other indications. Compounds of the invention include compounds having the formula (I) or a pharmaceutically acceptable salt thereof, wherein R1 to R8 are as defined herein.

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