Cas 96455-44-6,4-C-acetoxymethyl-4,8-anhydro-5,6,7,9-tetra-O-benzyl-2,3-dideoxy-D-glycero-D-ido-nonononitrile

96455-44-6

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Basic information

Product Name: 4-C-acetoxymethyl-4,8-anhydro-5,6,7,9-tetra-O-benzyl-2,3-dideoxy-D-glycero-D-ido-nonononitrile
Synonyms: 4-C-acetoxymethyl-4,8-anhydro-5,6,7,9-tetra-O-benzyl-2,3-dideoxy-D-glycero-D-ido-nonononitrile
CAS NO:96455-44-6
Molecular Formula:
Molecular Weight: 649.784
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: 4-C-acetoxymethyl-4,8-anhydro-5,6,7,9-tetra-O-benzyl-2,3-dideoxy-D-glycero-D-ido-nonononitrile(CAS DataBase Reference)
NIST Chemistry Reference: 4-C-acetoxymethyl-4,8-anhydro-5,6,7,9-tetra-O-benzyl-2,3-dideoxy-D-glycero-D-ido-nonononitrile(96455-44-6)
EPA Substance Registry System: 4-C-acetoxymethyl-4,8-anhydro-5,6,7,9-tetra-O-benzyl-2,3-dideoxy-D-glycero-D-ido-nonononitrile(96455-44-6)

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: 96455-44-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96455-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,5 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96455-44:
(7*9)+(6*6)+(5*4)+(4*5)+(3*5)+(2*4)+(1*4)=166
166 % 10 = 6
So 96455-44-6 is a valid CAS Registry Number.

96455-44-6Upstream product

96455-44-6Downstream Products

96455-44-6Relevant academic research and scientific papers

SYNTHESIS OF C-PENTO, -HEXO-, AND -HEPTULO-PYRANOSYL COMPOUNDS VIA RADICAL C-C BOND-FORMATION REACTIONS

Giese, Bernd,Dupuis, Jacques,Leising, Michael,Nix, Marianne,Lindner, Hans Joerg

, p. 329 - 341 (1987)

C-Glycosyl compounds were synthesized by addition of pyranosyl radicals to acrylonitrile, fumarodinitrile, or methacrylonitrile in the presence of tributyltin hydride in 34-75percent yields.The pyranosyl radicals were generated by abstraction of a bromine

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