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3770-60-3

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3770-60-3 Usage

Description

CHEMBRDG-BB 4017633 is a chemical compound that is not clearly identified in the public domain, therefore its specific properties and functions cannot be determined. Without further information, it is difficult to provide a detailed summary of the chemical.
Usage:
Since the specific properties and functions of CHEMBRDG-BB 4017633 cannot be determined due to the lack of information, it is not possible to list its uses or applications in different industries. Further information is required to provide a comprehensive understanding of its potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3770-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3770-60:
(6*3)+(5*7)+(4*7)+(3*0)+(2*6)+(1*0)=93
93 % 10 = 3
So 3770-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO/c1-5-2-3-7-6(4-5)10-8(9)11-7/h2-4H,1H3

3770-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-5-methyl-1,3-benzoxazole

1.2 Other means of identification

Product number -
Other names 2-CHLORO-5-METHYLBENZOXAZOLE

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:3770-60-3 SDS

3770-60-3Relevant articles and documents

A 2 - [d] oxazole chlorobenzene and -5 - preparation of formic acid method (by machine translation)

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Paragraph 0020; 0025; 0026, (2017/12/27)

The invention discloses a 2 - chlorobenzene and [d] oxazole - 5 - carboxylic acid, in order to 2 - nitro - 4 - methyl phenol as the starting material, passes through the reduction, ring, chlorinated, oxidation to obtain the target product, the compound is an important medical intermediates. (by machine translation)

NOVEL MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS REPLICATION

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, (2009/10/31)

The embodiments provide compounds of the general Formulae I, II, III, IV, V, VI, VII, and X, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.

Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor α agonists

Yamazaki, Yukiyoshi,Abe, Kazutoyo,Toma, Tsutomu,Nishikawa, Masahiro,Ozawa, Hidefumi,Okuda, Ayumu,Araki, Takaaki,Oda, Soichi,Inoue, Keisuke,Shibuya, Kimiyuki,Staels, Bart,Fruchart, Jean-Charles

, p. 4689 - 4693 (2008/02/11)

A combination of benzoxazole, phenoxyalkyl side chain, and phenoxybutyric acids was identified as a highly potent and selective human peroxisome proliferator-activated receptor α (PPARα) agonist. The synthesis, structure-activity relationship (SAR) studies, and in vivo activities of the representative compounds are described.

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