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603940-91-6

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603940-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 603940-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,9,4 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 603940-91:
(8*6)+(7*0)+(6*3)+(5*9)+(4*4)+(3*0)+(2*9)+(1*1)=146
146 % 10 = 6
So 603940-91-6 is a valid CAS Registry Number.

603940-91-6SDS

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 3-(5-Bromo-2-thienyl)alanine

1.2 Other means of identification

Product number -
Other names 2-amino-3-(4-tolyl)-1,4-naphthoquinone

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:603940-91-6 SDS

603940-91-6Upstream product

603940-91-6Downstream Products

603940-91-6Relevant articles and documents

Improved preparation of racemic 2-amino-3-(heteroaryl)propanoic acids and related compounds containing a furan or thiophene nucleus

Kitagawa, Tokujiro,Khandmaa, Dashrenchin,Fukumoto, Ayumi,Asada, Makoto

, p. 1137 - 1139 (2007/10/03)

Racemic 2-amino-3-(heteroaryl)propanoic acids (1), mostly with a furan or thiophene nucleus as a heteroaryl group, were synthesized in 48-94% yield by the reduction of 3-(heteroaryl)-2-(hydroxyimino)propanoic acids (5) with zinc dust and formic acid in the presence of a catalytic amount of iron dust at 60°C for 2 h. Under these conditions, unfavorable hydrogenolysis of bromine on the thiophene nucleus does not occur. Traditional Nformylation of the prepared 3-(heteroaryl)alanine (1) with a mixture of formic acid and acetic anhydride afforded 2-(formylamino)-3-(heteroaryl)propanoic acids (6) in 51-95% yield.

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