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662165-72-2

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662165-72-2 Usage

Family

Oxathiolane

Structure

Five-membered ring containing one oxygen and one sulfur atom

Substituent

4-chloro-3-nitrophenyl group

Chloro group

A chlorine atom attached to the phenyl ring

Nitro group

A nitro group (-NO2) attached to the phenyl ring

Potential applications

Pharmaceuticals, agrochemicals, and other industries

Reactivity

Unique structure and potential reactivity

Safety concerns

May pose risks to human health and the environment

Handling

Should be handled with caution due to potential risks

Check Digit Verification of cas no

The CAS Registry Mumber 662165-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,2,1,6 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 662165-72:
(8*6)+(7*6)+(6*2)+(5*1)+(4*6)+(3*5)+(2*7)+(1*2)=162
162 % 10 = 2
So 662165-72-2 is a valid CAS Registry Number.

662165-72-2SDS

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'-chloro-3'-nitrophenyl)-1,3-oxathiolane

1.2 Other means of identification

Product number -
Other names -

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:662165-72-2 SDS

662165-72-2Relevant articles and documents

Deprotection of 1,3-oxathiolanes to carbonyl compounds with montmorillonite K10

Chauhan,Kumar, Anil,Sahoo

, p. 2635 - 2637 (2007/10/03)

Montmorillonite K10 has been used in the deprotection of different aromatic and aliphatic 1,3-oxathiolanes to the corresponding carbonyl compounds in 73 to 97% yields under mild and environmentally compatible conditions.

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