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957187-34-7

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  • 6,9-Diazaspiro[4.5]decane-9-acetic acid, 8-(3,5-difluorophenyl)-10-oxo-, (8R)-

    Cas No: 957187-34-7

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957187-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 957187-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,1,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 957187-34:
(8*9)+(7*5)+(6*7)+(5*1)+(4*8)+(3*7)+(2*3)+(1*4)=217
217 % 10 = 7
So 957187-34-7 is a valid CAS Registry Number.

957187-34-7SDS

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 6,9-Diazaspiro[4.5]decane-9-acetic acid, 8-(3,5-difluorophenyl)-10-oxo-, (8R)-

1.2 Other means of identification

Product number -
Other names 6,9-DIAZASPIRO[4.5]DECANE-9-ACETIC ACID, 8-(3,5-DIFLUOROPHENYL)-10-OXO-, (8R)-

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:957187-34-7 SDS

957187-34-7Downstream Products

957187-34-7Relevant articles and documents

Practical asymmetric synthesis of a chiral piperazinone derivative

McLaughlin, Mark,Belyk, Kevin,Chen, Cheng-Yi,Linghu, Xin,Pan, Jun,Qian, Gang,Reamer, Robert A.,Xu, Yingju

, p. 1052 - 1060 (2013/09/12)

A practical asymmetric route to a chiral piperazinone derivative, a fragment of MK-3207, is reported. The amine-bearing benzylic stereocenter is introduced via an asymmetric Pd-catalyzed hydrogenation of a cyclic sulfimidate in the presence of a chiral phosphine ligand. An efficient synthesis of the hydrogenation substrate is described, together with process development of the hydrogenation step and elaboration of the resulting cyclic sulfamate product to the desired piperazinone.

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