Cas 1032290-72-4,p-methoxyphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-trio-O-benzyl-α-D-mannopyranoside

1032290-72-4

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Basic information

Product Name: p-methoxyphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-trio-O-benzyl-α-D-mannopyranoside
Synonyms: p-methoxyphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-trio-O-benzyl-α-D-mannopyranoside
CAS NO:1032290-72-4
Molecular Formula:
Molecular Weight: 1511.81
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: p-methoxyphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-trio-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-methoxyphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-trio-O-benzyl-α-D-mannopyranoside(1032290-72-4)
EPA Substance Registry System: p-methoxyphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1->2)-3,4,6-trio-O-benzyl-α-D-mannopyranoside(1032290-72-4)

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: 1032290-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032290-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,2,9 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1032290-72:
(9*1)+(8*0)+(7*3)+(6*2)+(5*2)+(4*9)+(3*0)+(2*7)+(1*2)=104
104 % 10 = 4
So 1032290-72-4 is a valid CAS Registry Number.

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1032290-72-4Relevant academic research and scientific papers

Sequential one-pot glycosidations catalytically promoted: Unprecedented strategy in oligosaccharide synthesis for the straightforward assemblage of the antitumor PI-88 pentasaccharide

Valerio, Silvia,Pastore, Antonello,Adinolfi, Matteo,Iadonisi, Alfonso

, p. 4496 - 4503 (2008/09/21)

(Chemical Equation Presented) The pentasaccharide sequence of the most active components of the antitumor drug PI-88, currently in phase II clinical trial, has been rapidly assembled in high overall yield and in only three steps starting from three monosa

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