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AMINO-BENZO[B]THIOPHEN-3-YL-ACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95834-55-2

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95834-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95834-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,3 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95834-55:
(7*9)+(6*5)+(5*8)+(4*3)+(3*4)+(2*5)+(1*5)=172
172 % 10 = 2
So 95834-55-2 is a valid CAS Registry Number.

95834-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Amino(1-benzothiophen-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-benzo[b]thiophenecarbonyl chloride

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:95834-55-2 SDS

95834-55-2Relevant academic research and scientific papers

Conformationally-restricted amino acid analogues bearing a distal sulfonic acid show selective inhibition of system xc- over the vesicular glutamate transporter

Etoga, Jean-Louis G.,Ahmed, S. Kaleem,Patel, Sarjubhai,Bridges, Richard J.,Thompson, Charles M.

scheme or table, p. 2680 - 2683 (2010/07/13)

A panel of amino acid analogs and conformationally-restricted amino acids bearing a sulfonic acid were synthesized and tested for their ability to preferentially inhibit the obligate cysteine-glutamate transporter system xc- versus t

Orally absorbable cephalosporin antibiotics. 3. Preparation of biologically active R isomer of 7-(3-benzothienylglycylamido)deacetoxycephalosporanic acid

Kukolja,Pfeil,Draheim,Ott

, p. 1903 - 1906 (2007/10/02)

The methyl and isopropyl esters of (RS)-3-benzothienylglycine were resolved with (+)- and (-)-tartaric acid in acetonitrile to give the corresponding R and S salts. The R-salt was hydrolyzed to (R)-3-benzothienylglycine (5). The amino group in 5 was prote

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