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4'-METHYLPHENYL 2-ACETAMIDO-3,4,6-TRI-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38229-73-1

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38229-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38229-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38229-73:
(7*3)+(6*8)+(5*2)+(4*2)+(3*9)+(2*7)+(1*3)=131
131 % 10 = 1
So 38229-73-1 is a valid CAS Registry Number.

38229-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,4R,5R,6S)-5-acetamido-3,4-diacetyloxy-6-(4-methylphenoxy)oxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names HMS654O02

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:38229-73-1 SDS

38229-73-1Downstream Products

38229-73-1Relevant academic research and scientific papers

Synthesis of N-Acetylglucosamine Aryl β-Glycosides Catalyzed by Crown Compounds

Kur'yanov,Chupakhina,Zemlyakov,Kotlyar,Kamalov,Chirva

, p. 385 - 389 (2007/10/03)

Glycosylation of various phenols with α-D-glucosaminyl chloride peracetate in a solid phase-liquid system catalyzed by crown compounds was studied. The highest yields of aryl β-glycosides were observed at room temperature in acetonitrile using anhydrous p

Carbohydrate protein interactions. Syntheses of agglutination inhibitors of wheat germ agglutinin by phase transfer catalysis

Roy, Rene,Tropper, Francois D.

, p. 817 - 821 (2007/10/02)

Starting from chloride 1, a series of para-substituted aryl 2-acetamido-2-deoxy-β-D-glucopyranosides were prepared using phase transfer catalysis conditions with tetrabutylammonium hydrogen sulfate in 1 M sodium hydroxide and methylene chloride at room temperature.Zemplen de-O-acetylation afforded the unprotected glycosides.Optimization of reaction conditions was evaluated.Several functional group manipulations were effected to widen the number and nature of the para-substituents. Key words: phase transfer catalysis, aryl 2-acetamido-2-deoxy-β-D-glucopyranosides.

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