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102719-10-8

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102719-10-8 Usage

Description

.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)is a complex chemical compound derived from hexopyranos, featuring an anhydro group and a phenylmethyl substituent. This rare sugar holds potential applications across various industries, including pharmaceuticals and the food additive sector, due to its unique structure and properties. Its exploration and development may pave the way for new breakthroughs in chemistry and related disciplines.

Uses

Used in Pharmaceutical Industry:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)is used as an active pharmaceutical ingredient for its potential therapeutic effects. Its unique molecular structure allows it to interact with biological targets, possibly leading to the development of new drugs for various medical conditions.
Used in Food Additive Industry:
In the food additive industry, .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)is used as a specialty ingredient to enhance the taste, texture, or shelf life of certain products. Its rare sugar properties may provide novel sensory experiences or health benefits when incorporated into the food supply.
Used in Chemical Research:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)is also utilized in chemical research as a model for studying the properties and reactivity of complex sugar derivatives. Its anhydro and phenylmethyl groups offer unique opportunities for understanding the behavior of such molecules in various chemical reactions and processes.
Used in Material Science:
The potential applications of .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)extend to material science, where its unique structure could be harnessed to develop new materials with specific properties, such as improved biocompatibility or enhanced mechanical strength.

Check Digit Verification of cas no

The CAS Registry Mumber 102719-10-8 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 102719-10:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*0)=88
88 % 10 = 8
So 102719-10-8 is a valid CAS Registry Number.

102719-10-8SDS

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 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose

1.2 Other means of identification

Product number -
Other names 1,6-anhydro-4-O-benzyl-β-D-erythro-hexopyranose-2-ulose

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:102719-10-8 SDS

102719-10-8Relevant articles and documents

Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation

Biktagirov,Faizullina,Salikhov,Safarov,Valeev

, p. 1317 - 1322 (2015/01/08)

4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy deri

Factors Affecting Reaction of 1,6-Anhydrohexos-2-ulose Derivatives

Kawai, Takatoshi,Isobe, Minoru,Peters, Steven C.

, p. 115 - 132 (2007/10/02)

1,6-Anhydrohexos-2-ulose derivatives undergo reaction with (trimethylsilyl)diazomethane in the presence of boron trifluoride etherate to afford structurally isomeric products.Ion-dipole interactions involving the 1,6-anhydro bridge and C4 substituents con

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