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2-O-glucopyranosylribitol-4'-phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121496-69-3

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121496-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121496-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,9 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121496-69:
(8*1)+(7*2)+(6*1)+(5*4)+(4*9)+(3*6)+(2*6)+(1*9)=123
123 % 10 = 3
So 121496-69-3 is a valid CAS Registry Number.

121496-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,4R,5R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2S,3R,4R)-1,3,4,5-tetrahydroxypentan-2-yl]oxyoxan-3-yl] dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names 2-O-Glucopyranosylribitol-4'-phosphate

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:121496-69-3 SDS

121496-69-3Downstream Products

121496-69-3Relevant academic research and scientific papers

The synthesis of two repeating units of Haemophilus influenzae type a capsular antigen.

Grzeszczyk,Banaszek,Zamojski

, p. 215 - 226 (2007/10/02)

The repeating units 2-O-beta-D-glucopyranosyl-L-ribitol 4'- and 1-phosphate of Haemophilus influenzae type a capsular antigen have been synthesised by condensation of an alpha-D-glucopyranosyl bromide derivative with 5-O-allyl-1,2,3-tri-O-benzyl-D-ribitol followed by selective deprotection of HO-4' or HO-1, phosphorylation, and removal of the blocking groups.

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