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56072-67-4

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56072-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56072-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,7 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56072-67:
(7*5)+(6*6)+(5*0)+(4*7)+(3*2)+(2*6)+(1*7)=124
124 % 10 = 4
So 56072-67-4 is a valid CAS Registry Number.

56072-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name oxolane-2,3-diol

1.2 Other means of identification

Product number -
Other names 2.3-Dihydroxy-tetrahydrofuran

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:56072-67-4 SDS

56072-67-4Downstream Products

56072-67-4Relevant articles and documents

A chemoenzymatic synthesis of deoxy sugar esters involving stereoselective acetylation of hemiacetals catalyzed by CALB

Villo, Ly,Kreen, Malle,Kudryashova, Marina,Metsala, Andrus,Tamp, Sven,Lille, Uelo,Pehk, Tonis,Parve, Omar

experimental part, p. 44 - 51 (2011/07/30)

An extension of the scope of the chemoenzymatic strategy for the synthesis of stereochemically pure pyranose deoxy sugar esters of different carboxylic acids has been achieved. The objective of the work was to extend the strategy to the synthesis of furanose deoxy sugar derivatives and additionally, to N-Boc-protected amino acid esters. With all used carboxylic acids (deoxycholic acid, α-methoxyphenylacetic acid, N-Boc-l-phenylalanine and N-Boc-l-tyrosine) the lipase-catalyzed stereoselective acetylation of furanose or pyranose hemiacetal moiety as a key step afforded one desired stereochemically pure acetylated hemiacetal deoxy sugar ester in high de.

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