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112339-36-3

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112339-36-3 Usage

General Description

.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, 4-methylbenzenesulfonate is a chemical compound that belongs to the class of arabinose derivatives. It is a derivative of a hexopyranose with a sulfonate group and a phenylmethyl group attached to it. .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, 4-methylbenzenesulfonate has potential applications in the field of medicinal chemistry and drug development. The presence of the sulfonate group and the phenylmethyl group can alter the chemical and physical properties of the parent hexopyranose, making it a potentially useful building block for the synthesis of new drugs and pharmaceutical compounds. Additionally, its unique structure and properties may also make it suitable for use in organic synthesis and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 112339-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,3 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112339-36:
(8*1)+(7*1)+(6*2)+(5*3)+(4*3)+(3*9)+(2*3)+(1*6)=93
93 % 10 = 3
So 112339-36-3 is a valid CAS Registry Number.

112339-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-anhydro-4-O-benzyl-3-deoxy-2-O-p-toluenesulphonyl-β-D-arabino-hexopyranose

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112339-36-3 SDS

112339-36-3Relevant 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

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