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2-Methylphenyl β-D-glucopyranoside 2,3,4,6-tetraacetate is a complex organic compound with the molecular formula C19H24O10. It is a derivative of phenyl β-D-glucopyranoside, where the hydroxyl groups at positions 2, 3, 4, and 6 of the glucose molecule are acetylated, resulting in the formation of acetate esters. 2-Methylphenyl β-D-glucopyranoside 2,3,4,6-tetraacetate is often used in organic synthesis and as a substrate in enzymatic reactions, particularly in the study of glycosidases. The 2-methylphenyl group attached to the glucose moiety provides a unique structural feature that can influence the reactivity and selectivity of the compound in various chemical and biological processes.

5346-66-7

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5346-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5346-66-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5346-66:
(6*5)+(5*3)+(4*4)+(3*6)+(2*6)+(1*6)=97
97 % 10 = 7
So 5346-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H26O10/c1-11-8-6-7-9-16(11)30-21-20(29-15(5)25)19(28-14(4)24)18(27-13(3)23)17(31-21)10-26-12(2)22/h6-9,17-21H,10H2,1-5H3

5346-66-7SDS

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 o-Cresol-.β.-D-glucoside tetraacetate

1.2 Other means of identification

Product number -
Other names o-Kresoxyacetylchlorid

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:5346-66-7 SDS

5346-66-7Relevant academic research and scientific papers

Selective demethylation ofO-aryl glycosides by iridium-catalyzed hydrosilylation

Jones, Caleb A. H.,Schley, Nathan D.

supporting information, p. 5953 - 5956 (2021/06/18)

The cleavage of alkyl ethers by hydrosilylation is a powerful synthetic tool for the generation of silyl ethers. Previous attempts to apply this transformation to carbohydrate derivatives have been constrained by poor selectivity and preferential reductio

CHELATION CONTROLLED REGIOSELECTIVE ALKYLATION AND 1,4 CHIRALITY TRANSFER IN OPTICALLY ACTIVE 1-ALKOXY-1,4-CYCLOHEXADIENES

Stanssens, Dirk,Keukeleire, Denis De,Vandewalle, Maurits

, p. 4195 - 4198 (2007/10/02)

Chelation controlled alkylation of optically active 1-alkoxy-1,4-cyclohexadienes leads to a mixture of 1,4-cyclohexadienes 4a-c and 1,3-cyclohexadienes 5a-c.The regio- and diastereoselectivities depend upon the nature of the chiral auxiliary and the react

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