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76003-45-7

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76003-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76003-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76003-45:
(7*7)+(6*6)+(5*0)+(4*0)+(3*3)+(2*4)+(1*5)=107
107 % 10 = 7
So 76003-45-7 is a valid CAS Registry Number.

76003-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (2R)-2-fluorobutanedioate

1.2 Other means of identification

Product number -
Other names Butanedioicacid,fluoro-,dimethyl ester,(R)-(9CI)

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:76003-45-7 SDS

76003-45-7Upstream product

76003-45-7Downstream Products

76003-45-7Relevant articles and documents

Synthesis, Absolute Configuration, and Circular Dichroism of the Enantiomers of Fluorosuccinic Acid

Lowe, Gordon,Potter, Barry V. L.

, p. 2029 - 2032 (2007/10/02)

Diethylaminosulphur trifluoride (DAST) converts (2S)- and (2R)-malate esters into the enantiomeric fluorosuccinate esters. (2S,3R)-Malate, obtained from fumarate by fumarase-catalysed hydration in deuterium oxide, was used to show that the reaction with DAST occurs stereospecifically with inversion of configuration.Conversion of (2S)-aspartic acid into fluorosuccinate with sodium nitrite in polyhydrogen fluoride-pyridine occurs predominantly with retention of configuration.The circular dichroic spectra of (2S)- and (2R)-fluorosuccinic acids and their methyl esters are 'anomalous' and consequently the absolute configuration previously assigned to a Pseudomonal metabolite, (+)-fluorosuccinic acid, is shown to be erroneous.

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