Cas 88152-92-5,1,6-anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-2'-O-(p-toluenesulfonyl)-β-maltose

88152-92-5

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Basic information

Product Name: 1,6-anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-2'-O-(p-toluenesulfonyl)-β-maltose
Synonyms: 1,6-anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-2'-O-(p-toluenesulfonyl)-β-maltose
CAS NO:88152-92-5
Molecular Formula:
Molecular Weight: 836.957
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1,6-anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-2'-O-(p-toluenesulfonyl)-β-maltose(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-2'-O-(p-toluenesulfonyl)-β-maltose(88152-92-5)
EPA Substance Registry System: 1,6-anhydro-2,3,3'-tri-O-benzyl-4',6'-O-benzylidene-2'-O-(p-toluenesulfonyl)-β-maltose(88152-92-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 88152-92-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88152-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,5 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88152-92:
(7*8)+(6*8)+(5*1)+(4*5)+(3*2)+(2*9)+(1*2)=155
155 % 10 = 5
So 88152-92-5 is a valid CAS Registry Number.

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88152-92-5Relevant academic research and scientific papers

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

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