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138582-72-6

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138582-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138582-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138582-72:
(8*1)+(7*3)+(6*8)+(5*5)+(4*8)+(3*2)+(2*7)+(1*2)=156
156 % 10 = 6
So 138582-72-6 is a valid CAS Registry Number.

138582-72-6SDS

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 (S)-3-Amino-N-(2-hydroxy-ethyl)-succinamic acid benzyl ester

1.2 Other means of identification

Product number -
Other names -

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:138582-72-6 SDS

138582-72-6Relevant articles and documents

SYNTHESIS OF A PEPTIDYLDIMANNOSYL PHOSPHATE: FRAGMENT OF THE VARIANT-SPECIFIC SURFACE GLYCOPROTEIN MEMBRANE ANCHOR FROM TRYPANOSOMA BRUCEI

Verduyn, R.,Belien, J. J. A.,Dreef-Tromp, C. M.,Marel, G. A. van der,Boom, J. H. van

, p. 6637 - 6640 (2007/10/02)

Condensation of protected β-benzyl-aspartate 4 with 2-amino-ethanol, subsequent deprotection of the amino function and coupling with N,N'-di-benzyloxycarbonyl-lysine (7) afforded the peptidyl alcohol 8.Glycosylation of methyl 3,4,6-tri-O-benzyl-α-D-mannopyranoside (11) by ethyl 2,6-di-O-benzoyl-3,4-di-O-benzyl-1-thio-α-D-mannopyranoside (14) gave, after debenzoylation and protection of the 2'-hydroxyl function, the suitably protected dimannoside 21.Phosphitylation of 21 with benzyloxy-bis-(N,N-diisopropylamino)phosphine (18) followed by the addition of 8 gave, after oxidation and subsequent hydrogenolysis of the benzyl groups, the title compound in a good yield.

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