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benzyl 2-(acetylamino)-3,4,6-tri-O-benzyl-2-deoxyhexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91927-50-3

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91927-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91927-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91927-50:
(7*9)+(6*1)+(5*9)+(4*2)+(3*7)+(2*5)+(1*0)=153
153 % 10 = 3
So 91927-50-3 is a valid CAS Registry Number.

91927-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]acetamide

1.2 Other means of identification

Product number -
Other names Galactose,2-acetamido-2-deoxy-1,3,4,6-tetrabenzyl

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:91927-50-3 SDS

91927-50-3Relevant academic research and scientific papers

GLYCOSIDASE INHIBITORS AND USES THEREOF

-

Paragraph 00143, (2014/03/25)

The invention provides compounds of Formula (I) for inhibiting gh cosidases, prodrugs of the compounds, and pharmaceutical compositions comprising the compounds or prodrugs of the compounds. The invention also provides method of treating diseases and diso

Regioselective removal of the anomeric O-benzyl from differentially protected carbohydrates

Jalsa, Nigel Kevin

supporting information; scheme or table, p. 6587 - 6590 (2012/02/03)

A mild, regioselective deprotection of the anomeric O-benzyl from multi-functionally protected carbohydrates via catalytic transfer hydrogenation is described. The protocol is tolerant of O-benzyl and O-benzylidene protections at non-anomeric positions, g

1,5-Dideoxy-1,5-imino-D-glucitol Compounds

-

Page/Page column 3, (2010/05/13)

1,5-Dideoxy-1,5-imino-D-glucitol compounds as shown in the specification. Also disclosed is a method of treating a hexosaminidase-associated disease.

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