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33493-71-9

33493-71-9

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33493-71-9 Usage

Chemical Properties

White to yellowish powder

Check Digit Verification of cas no

The CAS Registry Mumber 33493-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33493-71:
(7*3)+(6*3)+(5*4)+(4*9)+(3*3)+(2*7)+(1*1)=119
119 % 10 = 9
So 33493-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C34H35NO6/c1-24(36)35-30-32(38)31(37)29(41-33(30)39-22-25-14-6-2-7-15-25)23-40-34(26-16-8-3-9-17-26,27-18-10-4-11-19-27)28-20-12-5-13-21-28/h2-21,29-33,37-38H,22-23H2,1H3,(H,35,36)/t29-,30-,31-,32-,33+/m1/s1

33493-71-9SDS

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 N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-2-phenylmethoxy-6-(trityloxymethyl)oxan-3-yl]acetamide

1.2 Other means of identification

Product number -
Other names Benzyl 2-acetamido-2-deoxy-6-O-trityl-a-D-glucopyranoside

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:33493-71-9 SDS

33493-71-9Relevant articles and documents

The cobalt-catalyzed oxygenative radical route from hexopyranosides to carbapentofuranoses

Desire, Jerome,Prandi, Jacques

, p. 3075 - 3084 (2007/10/03)

Cobalt-catalyzed radical cyclization/oxygenation of various 6-iodohex-1-enitols gave in one step the carbocyclic analogs of pentofuranoses. The reaction was run under very mild conditions and gave moderate to good yields of carbapentofuranoses within a few hours. All the possible 6-iodohex-1-enitol stereoisomers were prepared, and the influence of relative configurations and protecting groups was studied.

Preparation of the 3,4-di-O-benzyl and 3,4-di-O-(4-phenylbenzyl) derivatives of benzyl 2-acetamido-2-deoxy-α-D-glucopyranoside

Vleugel, Dominicus J. M. van der,Vliegenthart, Johannes F. G.

, p. 168 - 172 (2007/10/02)

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