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34621-75-5

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34621-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34621-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34621-75:
(7*3)+(6*4)+(5*6)+(4*2)+(3*1)+(2*7)+(1*5)=105
105 % 10 = 5
So 34621-75-5 is a valid CAS Registry Number.

34621-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2S,3R,4R,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(2R,3R,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]acetamide

1.2 Other means of identification

Product number -
Other names Receptor for pili of Pseudomonas aeruginosa

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:34621-75-5 SDS

34621-75-5Downstream Products

34621-75-5Relevant academic research and scientific papers

SYNTHESE VON TRISACCHARID-EINHEITEN DER KAPSELPOLYSACCHARIDE VON Streptococcus pneumoniae

Paulsen, Hans,Helpap, Bernd,Lorentzen, Jens Peter

, p. 173 - 198 (2007/10/02)

In the presence of silver silicate as promoter, the reaction of gycosyl bromides of 2-azido-2-deoxy-D-mannose with 1,6-anhydro-2,3-di-O-benzyl-β-D-glucopyranoside led to derivatives of the disaccharide β-D-ManpNAc-(1->4)-D-Glcp.The derivatives were activa

Chemical Modification of Maltose. VII. Synthesis of 4-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-D-glucopyranose (GlcNAcα1->4Glc)

Mori, Masami,Tejima, Setsuzo

, p. 1593 - 1600 (2007/10/02)

1,6-Anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-β-maltose (5), a maltose derivative having only one unprotected hydroxyl group at the C-2' position, was synthesized from 1,6-anhydro-4',6'-O-benzylidene-2'-O-tosyl-β-maltose (2) by benzylation followed

Bausteine von Oligosacchariden, XXII. Synthese der Trisaccharid-Sequenz α-D-GlcNAc-(1-4)-β-D-Gal-(1-4)-D-GlcNAc aus blutgruppenaktiven Substanzen

Paulsen, Hans,Schnell, Dagmar

, p. 333 - 345 (2007/10/02)

A directly stereoselective α-glycoside synthesis to oligosaccharides succeeds in the presence of AgClO4/Ag2CO3 in methylene chloride with the α-bromide 1 of 2-azido-2-desoxy-D-glucose.By reaction with 1 the disaccharides 3, 7a, 7b, 18 and the trisaccharid

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