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100236-26-8

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100236-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100236-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100236-26:
(8*1)+(7*0)+(6*0)+(5*2)+(4*3)+(3*6)+(2*2)+(1*6)=58
58 % 10 = 8
So 100236-26-8 is a valid CAS Registry Number.

100236-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-(2-Aminophenylthio)-2-phthalimidopropionsaeure

1.2 Other means of identification

Product number -
Other names 3-(o-aminophenyl)thio-2(R)-phthalimidopropionic acid

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:100236-26-8 SDS

100236-26-8Downstream Products

100236-26-8Relevant articles and documents

BENZAZEPINE-, BENZOXAZEPINE- AND BENZOTHIAZEPINE-N-ACETIC ACID DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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, (2008/06/13)

Compounds with neutral endopeptidase (NEP) inhibitory activity corresponding to the formula I STR1 in which R 1 is a lower alkoxy-lower-alkyl group whose lower alkoxy radical is substituted by a lower alkoxy group, or a phenyl-lower-alkyl or phenyloxy-lower-alkyl group which can optionally be substituted in the phenyl ring by lower alkyl, lower alkoxy or halogen, or a naphthyl-lower-alkyl group, A is CH 2, O or S,R 2 is hydrogen or halogen,R. sup.3 is hydrogen or halogen,R 4 is hydrogen or a group forming a biolabile ester, andR 5 is hydrogen or a group forming a biolabile ester, and the physiologically acceptable acid addition salts thereof.

Condensed, seven-membered ring compounds, their production and use

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, (2008/06/13)

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Synthesis and angiotensin converting enzyme inhibitory activity of 1,5-benzothiazepine and 1,5-benzoxazepine derivatives. I

Itoh,Kori,Inada,Nishikawa,Kawamatsu,Sugihara

, p. 1128 - 1147 (2007/10/02)

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