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64037-24-7

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64037-24-7 Usage

General Description

5-Chloro-N-methyl-2-benzoxazolamine is a chemical compound with the molecular formula C9H8ClNO. It is an organic compound containing a benzoxazolamine core structure that is substituted with a methyl group at the nitrogen atom and a chlorine atom at the 5-position. 5-Chloro-N-methyl-2-benzoxazolamine is used in various research and industrial applications and has been studied for its potential pharmacological properties. It is important to handle this compound with caution, following proper safety measures and protocols, due to its potential hazards and risks associated with handling and exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 64037-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64037-24:
(7*6)+(6*4)+(5*0)+(4*3)+(3*7)+(2*2)+(1*4)=107
107 % 10 = 7
So 64037-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2O/c1-10-8-11-6-4-5(9)2-3-7(6)12-8/h2-4H,1H3,(H,10,11)

64037-24-7SDS

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 5-chloro-N-methyl-1,3-benzoxazol-2-amine

1.2 Other means of identification

Product number -
Other names (5-Chlor-benzoxazol-2-yl)-methyl-amin

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:64037-24-7 SDS

64037-24-7Downstream Products

64037-24-7Relevant articles and documents

Utility of Nitrogen Extrusion of Azido Complexes for the Synthesis of Nitriles, Benzoxazoles, and Benzisoxazoles

Nimnual, Phongprapan,Tummatorn, Jumreang,Thongsornkleeb, Charnsak,Ruchirawat, Somsak

, p. 8657 - 8667 (2015/09/15)

The utility of the nitrogen extrusion reaction of azido complexes, generated in situ from the corresponding aldehydes or ketones with TMSN3 in the presence of ZrCl4 or TfOH, has been described. These azido complexes could undergo three different pathways, depending on the substrates. First, azido methanolate complexes or imine diazonium ions could lead to benzisoxazole products via an intramolecular nucleophilic substitution. Second, imine diazonium ions could also undergo either the elimination of proton to provide nitrile products in good to excellent yields or an aryl migration, followed by an intramolecular nucleophilic addition, to give benzoxazole products in good yields.

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