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102719-14-2

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102719-14-2 Usage

General Description

The chemical ".beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate" is a compound that belongs to the class of carbohydrates and is a derivative of arabinose. It is structurally similar to the sugar arabinose, but with a modification at the 1,6-anhydro-3-deoxy position and an acetate group attached at position 2. This chemical is commonly used in the pharmaceutical industry as a starting material for the synthesis of various drug compounds and can also be utilized in organic chemistry research for the study of carbohydrate derivatives. Due to its specific structure and properties, it has potential applications in drug development and chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 102719-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,1 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102719-14:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*4)=92
92 % 10 = 2
So 102719-14-2 is a valid CAS Registry Number.

102719-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-O-acetyl-1,6-anhydro-3-deoxy-β-D-arabino-hexopyranose

1.2 Other means of identification

Product number -
Other names Acetic acid (1R,2S,4S,5R)-2-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester

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:102719-14-2 SDS

102719-14-2Relevant articles and documents

Manipulating the enone moiety of levoglucosenone: 1,3-Transposition reactions including ones leading to isolevoglucosenone

Ma, Xinghua,Liu, Xin,Yates, Patrick,Raverty, Warwick,Banwell, Martin G.,Ma, Chenxi,Willis, Anthony C.,Carr, Paul D.

, p. 5000 - 5011 (2018/06/20)

The manipulation of the enone moiety associated with the biomass-derived, homochiral and now abundant compound levoglucosenone (1) is described. While the trichloroacetimidates derived from the allylic alcohols 3 and 4 failed to engage in Overman-type rea

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