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102719-15-3

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102719-15-3 Usage

General Description

.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate, also known as acetylated anhydroerythritol, is a chemical compound that is derived from ribose, a type of sugar. It is a sugar alcohol that is acetylated and has a six-membered ring structure. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate is commonly used in organic synthesis and as a building block for the production of various pharmaceuticals and agrochemicals. It also has potential applications in the development of new materials and as a reagent in biochemical research. The acetylation of this compound enhances its stability and solubility, making it easier to handle and use in various chemical processes. Additionally, it may have potential biological activities and could be further studied for its potential medicinal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 102719-15-3 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 102719-15:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*5)=93
93 % 10 = 3
So 102719-15-3 is a valid CAS Registry Number.

102719-15-3SDS

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-ribo-hexopyranose

1.2 Other means of identification

Product number -
Other names Acetic acid (1R,2S,4R,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:102719-15-3 SDS

102719-15-3Relevant 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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