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29886-32-6

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29886-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29886-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29886-32:
(7*2)+(6*9)+(5*8)+(4*8)+(3*6)+(2*3)+(1*2)=166
166 % 10 = 6
So 29886-32-6 is a valid CAS Registry Number.

29886-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2S,3R,4R,5S,6R)-2-[(2R,3R,4S,5R)-5-acetamido-1,2,4,6-tetrahydroxyhexan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

1.2 Other means of identification

Product number -
Other names N,N inverted exclamation marka-Diacetylchitobiitol

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:29886-32-6 SDS

29886-32-6Relevant articles and documents

A METHOD FOR REDUCTIVE CLEAVAGE OF N-GLYCOSYLAMIDE CARBOHYDRATE-PEPTIDE BOND

Likhosherstov, Leonid M.,Novikova, Olga S.,Piskarev, Vladimir E.,Trusikhina, Elena E.,Derevitskaya, Varvara A.,Kochetkov, Nikolay K.

, p. 155 - 164 (2007/10/02)

A new, mild method for the splitting of N-linked oligosaccharides from glycoproteins includes treatment of glycoproteins (ovomucoid, flavoprotein, ribonuclease B, hemagglutinin, or transferrin) with 2 M LiBH4 in 25 mM LiOH - 50 mM Li citrate - 70percent aqueous tert-butyl alcohol (5 h, 45 deg C), followed by hydrolysis of the resulting glycosylamine with aqueous acetic acid.The oligosaccharides formed were easily isolated by gel filtration and cation-exchange chromatography in 60-80 percent yields.The reaction was accompanied by the intense reductive cleavage of peptide bonds with formation of amino alcohols, but N-deacetylation of hexosamine was completely excluded.The optimal conditions of this reaction were chosen by use of a model glycopeptide, 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1-N-(4-L-aspartoyl)-2-deoxy-β-D-glucopyranosylamine

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