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35351-20-3

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35351-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35351-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,5 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35351-20:
(7*3)+(6*5)+(5*3)+(4*5)+(3*1)+(2*2)+(1*0)=93
93 % 10 = 3
So 35351-20-3 is a valid CAS Registry Number.

35351-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-1-benzofuran-2-carboxamide

1.2 Other means of identification

Product number -
Other names 5-chloro-benzofuran-2-carboxylic acid amide

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:35351-20-3 SDS

35351-20-3Relevant articles and documents

A 5-substituted phenylpropyl furan-2-carboxylic acid and its derivative synthesis method

-

Paragraph 0051; 0052, (2016/11/21)

The invention discloses a synthesis method for 5-substituted benzofuran-2-carboxylic acid and the derivatives thereof. The synthesis method comprises the following steps of: 1) performing a chloromethylation reaction or a bromomethylation reaction on 4-substituted phenol to generate 2-halogenated methyl-4-substituted phenol; 2) reacting 2-halogenated methyl-4-substituted phenol with triphenylphosphine to generate 2-hydroxyl-5-substituted halogenated benzyltriphenyl phosphonium; 3) performing a ring-closing reaction on 2-hydroxyl-5-substituted halogenated benzyltriphenyl phosphonium and trichloroacetyl chloride in an alkaline condition to obtain 2-trichloromethyl-5-substituted benzofuran; and 4) performing alcoholysis on 2-trichloromethyl-5-substituted benzofuran in an acidic condition to obtain 5-substituted benzofuran-2-carboxylic ester, and then performing functional group conversion to obtain a series of derivatives. According to the synthesis method provided by the invention, cheap and easily-available raw materials are used, thus reducing production cost; and moreover, the synthesis method is simple and convenient in process, easy to enlarge, and high in implement value.

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