Cas 732296-49-0,benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside

732296-49-0

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Basic information

Product Name: benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside
Synonyms: benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside
CAS NO:732296-49-0
Molecular Formula:
Molecular Weight: 1032.15
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: benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside(732296-49-0)
EPA Substance Registry System: benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside(732296-49-0)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 732296-49-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 732296-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,2,2,9 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 732296-49:
(8*7)+(7*3)+(6*2)+(5*2)+(4*9)+(3*6)+(2*4)+(1*9)=170
170 % 10 = 0
So 732296-49-0 is a valid CAS Registry Number.

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732296-49-0Relevant academic research and scientific papers

Novel synthesis of disaccharides containing the 2-amino-2-deoxy-β-D- glucopyranosyl unit and L-Glycero-D-Manno- and 7-deoxy-L-Glycero-D-Galacto- heptopyranoses

Martin, Patrick,Lequart, Vincent,Cecchelli, Romeo,Boullanger, Paul,Lafont, Dominique,Banoub, Joseph

, p. 696 - 697 (2007/10/03)

Stereocontrolled syntheses of immunologically relevant heptopyranose disaccharides were achieved in excellent yields by the trimethylsilyl triflate promoted glycosylation of the donor 1,3,4,6-tetra-O-acetyl-2-N-allyloxycarbonyl- 2-amino-2-deoxy-β-D-glucop

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