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1041439-31-9

1041439-31-9

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1041439-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041439-31-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,4,3 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1041439-31:
(9*1)+(8*0)+(7*4)+(6*1)+(5*4)+(4*3)+(3*9)+(2*3)+(1*1)=109
109 % 10 = 9
So 1041439-31-9 is a valid CAS Registry Number.

1041439-31-9SDS

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 ethyl 3-benzyl-7-{[(4-methylphenyl)sulfonyl]oxy}-9-[(1R)-1-phenylethyl]-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 3-benzyl-9-((S)-1-phenylethyl)-7-(tosyloxy)-3,9-diazabicyclo3.3.1non-6-ene-6-carboxylate

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:1041439-31-9 SDS

1041439-31-9Downstream Products

1041439-31-9Relevant articles and documents

Practical synthesis of a renin inhibitor via a diastereoselective dieckmann cyclization

Gauvreau, Danny,Hughes, Greg J.,Lau, Stephen Y. W.,McKay, Daniel J.,O'Shea, Paul D.,Sidler, Rick R.,Yu, Bing,Davies, Ian W.

supporting information; experimental part, p. 5146 - 5149 (2011/02/23)

A scalable synthesis of a potent renin inhibitor (1) is described. The absolute stereochemistry is set via an unprecedented diastereoselective Dieckmann cyclization directed by a remote chiral protecting group. This transformation enables preparation of chiral 1,3-[3.3.1]-diazabicyclononenes by desymmetrization of alkyl-esters, with selectivities ranging from 4 to 17:1.

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