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147976-18-9

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147976-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147976-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,9,7 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 147976-18:
(8*1)+(7*4)+(6*7)+(5*9)+(4*7)+(3*6)+(2*1)+(1*8)=179
179 % 10 = 9
So 147976-18-9 is a valid CAS Registry Number.

147976-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,5S)-4-benzyl-2-oxo-oxazolidine-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names (4S,5S)-4-benzyl-oxazolidin-2-one-5-carboxylic acid

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:147976-18-9 SDS

147976-18-9Relevant articles and documents

Facile synthetic route to (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid and its derivatives, the key intermediates for HIV protease inhibitors

Lei, Lijun,He, Xuchang,Bai, Donglu

, p. 1535 - 1540 (2007/10/03)

A facile and efficient route to (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid and its derivative (4S,5S)-4-benzyl-5-hydroxymethyl oxazolidin-2-one is presented. N-phthaloyl protected L-phenylalanine 1 was treated with thionyl chloride followed by hydroge

Process for the production of a β-amino alcohol

-

, (2008/06/13)

A process for producing 2-?3(S)-amino-2-(R)-hydroxyl-4-phenyl butyl!-N-tert,butyl decahydro-(4aS,8aS)-isoquinoline-e(S)-carboxamide of the formula (I) via 3(S)-?lower alkoxy carbonyl amino, phenoxy carbonyl amino or benzyl oxycarbonyl amino!-2-hydroxy-4-phenyl butyric acid and process for producing said acid.

Enantiomerically pure 3-amino-2-hydroxy and 5-amino-4-hydroxy acids from D-isoascorbic acid

Melon, D.,Gravier-Pelletier, C.,Merrer, Y. Le,Depezay, J. C.

, p. 585 - 593 (2007/10/02)

The chirospecific synthesis of 3-amino-2-hydroxy aldehyde or acid units is an important issue in the context of synthetic strategies directed towards the construction of biologically relevant target molecules such as amino sugars, antibiotics, enzyme inhi

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