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2495-96-7

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2495-96-7 Usage

General Description

ETHYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a chemical compound with a molecular formula of C10H19NO7. It is a derivative of glucose and belongs to the family of glycosides. ETHYL 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is commonly used in the pharmaceutical industry as a building block for the synthesis of various drug molecules, particularly antibiotics and antiviral agents. It has also shown potential as a promising candidate for the development of new treatments for bacterial and viral infections. Additionally, it has been studied for its potential antioxidant and anti-inflammatory properties, making it a versatile compound with various potential applications in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 2495-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2495-96:
(6*2)+(5*4)+(4*9)+(3*5)+(2*9)+(1*6)=107
107 % 10 = 7
So 2495-96-7 is a valid CAS Registry Number.

2495-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-ethoxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

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

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

More Details:2495-96-7 SDS

2495-96-7Downstream Products

2495-96-7Relevant articles and documents

PRODUCTION METHOD OF ALKYL N-ACETYLGLUCOSAMINIDE

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Paragraph 0041, (2016/12/01)

PROBLEM TO BE SOLVED: To provide a method for obtaining alkyl N-acetylglucosaminide that comprises few content of N-acetyl glucosamine as impurities, conveniently and efficiently with a low cost. SOLUTION: The invention provides a production method of alkyl N-acetylglucosaminide comprising a step of reducing the content of N-acetyl glucosamine by contacting a mixture of alkyl N-acetylglucosaminide and N-acetyl glucosamine with strongly basic anion exchange resin (where, alkyl means an alkyl group of carbon number 1-4). The invention relates to the production method of alkyl N-acetylglucosaminide which is a mixture of alkyl N-acetylglucosaminide and N-acetyl glucosamine obtained by reaction of N-acetyl glucosamine, chitin, or chitin oligosaccharide with alkyl alcohol under the presence of an acid, or transglycosidation of chitin or chitin oligosaccharide using an enzyme with N-acetylhexosaminidase activity in a mixed solution of alkyl alcohol and water. COPYRIGHT: (C)2016,JPOandINPIT

HELICOBACTER PYLORI BACTERIUM PROLIFERATION INHIBITOR

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Page/Page column 5, (2011/08/04)

The present invention herein provides a proliferation inhibitor of H. pylori bacteria comprising a compound that can specifically inhibit the proliferation of H. pylori bacteria, which does not generate bacterium resistant, can be eaten, drunken or administrated safely for a long period of time, can be simply mass-manufactured and can be used for foods and beverages or pharmaceutical preparation. The proliferation inhibitor of H. pylori bacteria comprises an N-acetylglucosaminyl beta-linked monosaccharide derivative represented by the following chemical formula (1): ????????GlcNAc1-beta-O-Y?????(1) wherein Y is an alkyl group, an alkoxyl group, an alkenyl group, an alkynyl group, an aralkyl group, an aryl group, a heteroaryl group, a carboxyl group or an alkoxycarbonyl group.

Resolution of anomeric ethyl 2-amino-2-deoxy-D-glucopyranoside by cation-exchange chromatography, and its N-acylation with carboxylic anhydrides.

Hirano,Ishigami,Ohe

, p. 4038 - 4040 (2007/10/04)

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