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1,3,4,6-tetra-O-acetyl-2-[acetyl(methyl)amino]-2-deoxyhexopyranose is a complex organic compound with the molecular formula C16H23NO9. It is a derivative of a hexopyranose sugar, specifically a 2-deoxyhexopyranose, which has been modified with various functional groups. The compound features four acetyl groups (-COCH3) attached to the 1, 3, 4, and 6 positions of the hexopyranose ring, which protect the hydroxyl groups and increase its stability. Additionally, a methylamino group (-NHCH3) is present at the 2 position, which is also acetylated, forming an acetyl(methyl)amino group. 1,3,4,6-tetra-O-acetyl-2-[acetyl(methyl)amino]-2-deoxyhexopyranose is of interest in the field of carbohydrate chemistry, as it represents a modified sugar that can be used in the synthesis of various biologically active molecules and pharmaceuticals. Its complex structure and functional groups make it a valuable compound for studying the properties and reactivity of modified sugars.

7460-96-0

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7460-96-0 Usage

Chemical structure

A complex chemical compound with a hexose sugar (2-deoxyhexopyranose) as the core structure.

Acetylation

The hexose sugar is acetylated at positions 1, 3, 4, and 6, which increases its reactivity and stability.

Amino group

An acetyl(methyl)amino group is attached to the molecule, providing additional functionality and reactivity.

Derivative of glucose

It is a derivative of glucose, a common monosaccharide found in living organisms.

Organic chemistry applications

Widely used in organic chemistry for its reactivity and unique properties.

Synthesis

Utilized in the synthesis of other compounds and as a building block for various chemical reactions.

Pharmaceutical applications

Has potential applications in the pharmaceutical industry, particularly in drug development and research.

Carbohydrate chemistry

Relevant to carbohydrate chemistry, as it is a modified sugar molecule with unique properties.

Solubility

Likely soluble in organic solvents such as chloroform, acetone, and methanol due to its acetylated and amino substituents.

Stability

The acetyl groups may increase the stability of the molecule, protecting the sugar from hydrolysis and enzymatic degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 7460-96-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7460-96:
(6*7)+(5*4)+(4*6)+(3*0)+(2*9)+(1*6)=110
110 % 10 = 0
So 7460-96-0 is a valid CAS Registry Number.

7460-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-[acetyl(methyl)amino]-3,4,6-triacetyloxyoxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names N-Methyl-2-acetamido-2-deoxy-1,3,4,6-tetra-O-acetyl-L-glucopyranose

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:7460-96-0 SDS

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