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Methyl 4-O-acetylhexopyranoside is a chemical compound that belongs to the class of hexopyranosides, which are derivatives of hexoses, a type of sugar. This specific compound features a methyl group attached to the anomeric carbon (the first carbon in the sugar ring) and an acetyl group (an ester of acetic acid) at the 4-O position, indicating it is attached to the fourth oxygen atom in the sugar ring. The presence of the acetyl group provides the molecule with additional functionality and reactivity, which can be useful in various chemical reactions and synthetic pathways. Methyl 4-O-acetylhexopyranoside is often used in organic synthesis, particularly in the preparation of complex carbohydrates and as a building block for the synthesis of more intricate molecular structures.

6340-54-1

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6340-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6340-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6340-54:
(6*6)+(5*3)+(4*4)+(3*0)+(2*5)+(1*4)=81
81 % 10 = 1
So 6340-54-1 is a valid CAS Registry Number.

6340-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [4,5-dihydroxy-2-(hydroxymethyl)-6-methoxyoxan-3-yl] acetate

1.2 Other means of identification

Product number -
Other names methyl 4-O-acetylhexopyranoside

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:6340-54-1 SDS

6340-54-1Relevant academic research and scientific papers

Acetyl Group Migration across the Saccharide Units in Oligomannoside Model Compound

Lassfolk, Robert,Rahkila, Jani,Johansson, Mikael P.,Ekholm, Filip S.,W?rn?, Johan,Leino, Reko

, p. 1646 - 1654 (2019/01/21)

Acetylated oligosaccharides are common in nature. While they are involved in several biochemical and biological processes, the role of the acetyl groups and the complexity of their migration has largely gone unnoticed. In this work, by combination of organic synthesis, NMR spectroscopy and quantum chemical modeling, we show that acetyl group migration is a much more complex phenomenon than previously known. By use of synthetic oligomannoside model compounds, we demonstrate, for the first time, that the migration of acetyl groups in oligosaccharides and polysaccharides may not be limited to transfer within a single monosaccharide moiety, but may also involve migration over a glycosidic bond between two different saccharide units. The observed phenomenon is not only interesting from the chemical point of view, but it also raises new questions about the potential biological role of acylated carbohydrates in nature.

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