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148705-04-8

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148705-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148705-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,7,0 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 148705-04:
(8*1)+(7*4)+(6*8)+(5*7)+(4*0)+(3*5)+(2*0)+(1*4)=138
138 % 10 = 8
So 148705-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C38H41NO17S/c1-18(40)48-16-27-31(51-21(4)43)33(52-22(5)44)34(53-23(6)45)37(54-27)56-32-29(39-35(46)25-14-10-11-15-26(25)36(39)47)38(57-24-12-8-7-9-13-24)55-28(17-49-19(2)41)30(32)50-20(3)42/h7-15,27-34,37-38H,16-17H2,1-6H3/t27-,28-,29-,30-,31+,32-,33+,34-,37+,38+/m1/s1

148705-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,4S,5R,6R)-3,4,5-triacetyloxy-6-[(2R,3S,4R,5R,6S)-3-acetyloxy-2-(acetyloxymethyl)-5-(1,3-dioxoisoindol-2-yl)-6-phenylsulfanyloxan-4-yl]oxyoxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names Phenyl tacgal-sglu

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:148705-04-8 SDS

148705-04-8Relevant articles and documents

A convenient synthesis of lacto-N-biose I [β-D-Galp-(1 → 3)-β-D-GlcpNAc] linkd oligosaccharides from phenyl O-(tetra-O-acetyl-β-D-galactopyranosyl)-(1 → 3)-4,6-di-O-acetyl-2-deoxy-2-phthalmido-1-thio-β-D-glucopyranoside

Jain,Locke,Matta

, p. 165 - 176 (2007/10/02)

The synthesis of two tetrasaccharides and one trisaccharide containing lacto-N-biose I (β-D-Galp(1 → 3)-β-D-GlcpNAc) as their terminal unit was accomplished through development and utilization of a key glycosyl donor, namely, phenyl O-(2,3,4,6-tetra-O-ace

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