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79778-31-7

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79778-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79778-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,7 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79778-31:
(7*7)+(6*9)+(5*7)+(4*7)+(3*8)+(2*3)+(1*1)=197
197 % 10 = 7
So 79778-31-7 is a valid CAS Registry Number.

79778-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-acetamido-3-carboxyprop-2-enyl)-(hydroxymethyl)-oxophosphanium

1.2 Other means of identification

Product number -
Other names 2-Butenoic acid,2-(acetylamino)-4-(hydroxymethylphosphinyl)

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:79778-31-7 SDS

79778-31-7Downstream Products

79778-31-7Relevant articles and documents

Enantioselective Synthesis of Both Enantiomers of Phosphinothricin via Asymmetric Hydrogenation of α-Acylamido Acrylates

Zeiss, Hans-Joachim

, p. 1783 - 1788 (2007/10/02)

Both enantiomers of phoshinothricin (1), a naturally occuring amino acid that contains the unique methylphosphinate moiety, were prepared by asymmetric hydrogenation of α-acylamido acrylate precursors 7.L-1 and peptides containing L-1 are inhibitors of the enzyme glutamine synthetase (GS).Inhibition of GS is responsible for the antibiotical and herbicidal properties of these compounds.Synthesis of substrates 7 and parameters influencing the enantioselectivity are discussed.Substrate concentration and solvent polarity appear to have the most marked effects on enantiomeric excesses for a given catalyst system.Enantiomeric excesses reach 91percent for hydrogenations with (R,R)-NORPHOS- and (S,S)-CHIRAPHOS-derived catalysts.

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