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141109-26-4

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141109-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141109-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,0 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141109-26:
(8*1)+(7*4)+(6*1)+(5*1)+(4*0)+(3*9)+(2*2)+(1*6)=84
84 % 10 = 4
So 141109-26-4 is a valid CAS Registry Number.

141109-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(2-chlorophenyl)-2-(2-thiophen-2-ylethylamino)acetate

1.2 Other means of identification

Product number -
Other names Methyla-[[2-(thien-2-yl)ethyl]amino]-a-(2-chlorophenyl)acetate

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:141109-26-4 SDS

141109-26-4Relevant articles and documents

Synthetic method of racemic clopidogrel

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Paragraph 0031-0032; 0034; 0038-0039; 0042-0043; 0045, (2020/09/12)

The invention relates to a synthesis method of racemic clopidogrel, which comprises the following steps: 1) uniformly mixing methyl benzoylformate, N-chlorosuccinimide, palladium acetate, a ligand andtrifluoroacetic acid, and carrying out ortho-chlorinati

Concise Synthesis of (±)-Clopidogrel via Carboxylation of Benzylamine with CO2

Venkataramasubramanian,Sudalai, Arumugam

, p. 2099 - 2105 (2015/09/01)

A concise and efficient synthesis of (±)-clopidogrel, an antithrombotic agent, is achieved by inserting CO2 at the benzylic position as the key reaction without using any toxic transition metals. The overall yield of the synthetic process is 38% and the salient features include operationally simple process chemistry and fewer steps.

Process for the preparation of a pharmacologically active substance

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, (2008/06/13)

The present invention relates to a process for the preparation of the racemic or optically active compounds of general formula (VI): wherein the meaning of X is a halogen atom, or their salts, characterized in that, a racemic or optically active new compound of general formula (VII): wherein the meaning of X is a halogen atom, is transformed into the racemic or optically active compound of general formula (VIII):

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