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136755-18-5

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  • PENT-4-ENYL-6-O-T-BUTYLDIPHENYLSILYL-2,3,4-TRI-O-BENZOYL-D-GLUCOPYRANOSIDE

    Cas No: 136755-18-5

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136755-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136755-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,5 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136755-18:
(8*1)+(7*3)+(6*6)+(5*7)+(4*5)+(3*5)+(2*1)+(1*8)=145
145 % 10 = 5
So 136755-18-5 is a valid CAS Registry Number.
InChI:InChI=1/C48H50O9Si/c1-5-6-22-33-52-47-43(57-46(51)37-27-16-9-17-28-37)42(56-45(50)36-25-14-8-15-26-36)41(55-44(49)35-23-12-7-13-24-35)40(54-47)34-53-58(48(2,3)4,38-29-18-10-19-30-38)39-31-20-11-21-32-39/h5,7-21,23-32,40-43,47H,1,6,22,33-34H2,2-4H3/t40-,41-,42+,43-,47u/m1/s1

136755-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name PENT-4-ENYL-6-O-T-BUTYLDIPHENYLSILYL-2,3,4-TRI-O-BENZOYL-D-GLUCOPYRANOSIDE

1.2 Other means of identification

Product number -
Other names PENT-4-ENYL-6-O-T-BUTYLDIPHENYLSILYL-2,3,4-TRI-O-BENZOYLOXY-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:136755-18-5 SDS

136755-18-5Relevant articles and documents

Application of n-pentenyl glycosides in the regio- and stereo-controlled synthesis of α-linked N-glycopeptides

Ratcliffe,Konradsson,Reid

, p. 323 - 335 (2007/10/02)

The N-glycopeptides α-Glc-(1→Asn and α-Glc-(1→6)-β-Glc-(1→6)-α-Glc-(1→Asn have been synthesized efficiently from pent-4-enyl D-glucopyranoside derivatives. The methodology illustrates (a) a novel route for formation of the N-α-D-glucosyl-asparagine link,

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