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1307233-94-8

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  • Ethyl N-{[2-(chloromethyl)-1-methyl-1H-benzimidazol-5-yl]-carbonyl}-N-pyridin-2-yl-β-alaninate

    Cas No: 1307233-94-8

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1307233-94-8 Usage

Uses

Ethyl 3-(2-(Chloromethyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate is an intermediate used to synthesize dabigatran etexilate.

Check Digit Verification of cas no

The CAS Registry Mumber 1307233-94-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,7,2,3 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1307233-94:
(9*1)+(8*3)+(7*0)+(6*7)+(5*2)+(4*3)+(3*3)+(2*9)+(1*4)=128
128 % 10 = 8
So 1307233-94-8 is a valid CAS Registry Number.

1307233-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-[[2-(chloromethyl)-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoate

1.2 Other means of identification

Product number -
Other names N-[[2-(Chloromethyl)-1-methyl-1H-benzimidazol-5-yl]carbonyl]-N-2-pyridinyl-beta-alanine ethyl ester

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:1307233-94-8 SDS

1307233-94-8Relevant articles and documents

Preparation method of Pradaxa intermediate

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Paragraph 0022; 0023; 0024, (2018/11/03)

The invention belongs to the technical field of medicine preparation, and particularly relates to a preparation method of a Pradaxa intermediate. An adopted compound 6 has the characteristics of stable properties, no irritating odor, low price and the like. The defects that acid anhydride or acyl chloride compounds having the disadvantages of irritating odor, hygroscopicity and a high requirementfor an anhydrous reaction system are adopted in an existing synthesis route of the Pradaxa intermediate can be overcome. The reaction process has easier operation and control, high selectivity and stable yield.

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