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101094-63-7

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101094-63-7 Usage

Structure

A benzoxazole derivative containing a chlorobenzyl group and a thiol group.

Potential applications

Pharmaceutical, agrochemical, and material science industries.

Biological activity

Being studied for its potential use as a drug or pesticide.

Synthesis

May be used as a precursor for the synthesis of other organic compounds.

Research and development

Of interest in various fields due to its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 101094-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,9 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 101094-63:
(8*1)+(7*0)+(6*1)+(5*0)+(4*9)+(3*4)+(2*6)+(1*3)=77
77 % 10 = 7
So 101094-63-7 is a valid CAS Registry Number.

101094-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorobenzylsulfanyl)benzoxazole

1.2 Other means of identification

Product number -
Other names p-chlorobenzyl 2-benzoxazolyl sulfide

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:101094-63-7 SDS

101094-63-7Downstream Products

101094-63-7Relevant articles and documents

Electrooxidation of thiols in the presence of halide ions - A facile preparative method for synthesis of disulfides

Niyazymbetov,Konyushkin,Niyazymbetova,Litvinov,Petrosyan

, p. 1659 - 1665 (1993)

The aliphatic, aromatic and heteroaromatic disulfides were easily synthesized by the electrolysis of corresponding thiols. The electrochemical method is also convenient for synthesis of unsymmetrically substituted disulfides and 'paired' synthesis of disu

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