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76999-62-7

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76999-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76999-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,9 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76999-62:
(7*7)+(6*6)+(5*9)+(4*9)+(3*9)+(2*6)+(1*2)=207
207 % 10 = 7
So 76999-62-7 is a valid CAS Registry Number.

76999-62-7SDS

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 2,3-bis-benzoyloxy-propan-1-ol

1.2 Other means of identification

Product number -
Other names 1,2-Di-O-benzoyl-DL-glycerin

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:76999-62-7 SDS

76999-62-7Relevant articles and documents

NOVEL PREPARATION OF 1,3-PROPANEDIYL BIS: A ONE-STEP NUCLEOPHILIC SYNTHESIS OF SYMMETRIC 1,3-DIGLYCERIDES

Brown, Alan B.,Whitlock, Howard W.

, p. 3497 - 3508 (2007/10/02)

The title compound 1 was prepared by treatment of epibromohydrin with carboxylic acid 2 in the presence of tertiary amine; the reaction is a new nucleophilic synthesis of symmetric 1,3-diglycerides.

AN ASYMMETRIC SYNTHESIS OF GLYCEROL DERIVATIVES BY THE ENANTIOSELECTIVE ACYLATION OF PROCHIRAL GLYCEROL

Ichikawa, Junji,Asami, Masatoshi,Mukaiyama, Teruaki

, p. 949 - 952 (2007/10/02)

Optically active glycerol derivatives are obtained in up to 84percent e.e. by the selective acylation of the tin(II) alkoxides generated from 2-O-arylsulfonylglycerols and 1,1'-dimethylstannocene or (mehthylcyclopentadienyl)tin(II) chloride by the use of a chiral diamine derived from (S)-proline as a ligand.

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