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169774-81-6

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  • 3-Pyrrolidineacetic acid, 1-benzoyl-2-(methoxycarbonyl)-4-(3-methoxyphenyl)-, methyl ester, (2S,3S,4S)-

    Cas No: 169774-81-6

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169774-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169774-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,7,7 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 169774-81:
(8*1)+(7*6)+(6*9)+(5*7)+(4*7)+(3*4)+(2*8)+(1*1)=196
196 % 10 = 6
So 169774-81-6 is a valid CAS Registry Number.

169774-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,4S)-N-benzoyl-2-methoxycarbonyl-3-methoxycarbonylmethyl-4-(3-methoxyphenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names (2S,3S,4S)-1-Benzoyl-3-methoxycarbonylmethyl-4-(3-methoxy-phenyl)-pyrrolidine-2-carboxylic acid methyl 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:169774-81-6 SDS

169774-81-6Downstream Products

169774-81-6Relevant articles and documents

Towards a versatile synthesis of kainoids II: Two methods for establishment of C-4 stereochemistry

Baldwin, Jack E.,Bamford, Samantha J.,Fryer, Andrew M.,Rudolph, Martin P. W.,Wood, Mark E.

, p. 5255 - 5272 (2007/10/03)

Benzylic lactone hydrogenolysis and enamide reduction were used to generate protected C-4 aryl substituted kainoid analogues which were deprotected to their corresponding free amino acids. X-ray crystographic data were obtained for the C-4 2-MeOPh- analogue.

A versatile approach to acromelic acid analogues

Baldwin, Jack E.

, p. 4869 - 4872 (2007/10/02)

A route to acromelic acid analogues and their corresponding C-4 epimers from trans-4-hydroxy-L-proline is described. The C-4 substituent was introduced by a Suzuki-type boronate coupling to a vinyl triflate.

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