Cas 163456-99-3,N-benzyl-(6S,1'R,2'R,3'R,4'R)-6-(1',2',3'-tri-O-benzyl-4',5'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one

163456-99-3

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Basic information

Product Name: N-benzyl-(6S,1'R,2'R,3'R,4'R)-6-(1',2',3'-tri-O-benzyl-4',5'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one
Synonyms: N-benzyl-(6S,1'R,2'R,3'R,4'R)-6-(1',2',3'-tri-O-benzyl-4',5'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one
CAS NO:163456-99-3
Molecular Formula:
Molecular Weight: 647.811
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: N-benzyl-(6S,1'R,2'R,3'R,4'R)-6-(1',2',3'-tri-O-benzyl-4',5'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one(CAS DataBase Reference)
NIST Chemistry Reference: N-benzyl-(6S,1'R,2'R,3'R,4'R)-6-(1',2',3'-tri-O-benzyl-4',5'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one(163456-99-3)
EPA Substance Registry System: N-benzyl-(6S,1'R,2'R,3'R,4'R)-6-(1',2',3'-tri-O-benzyl-4',5'-O-isopropylidene-1',2',3',4',5'-pentahydroxy-1'-pentyl)-2,3-didehydropiperidine-4-one(163456-99-3)

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: 163456-99-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163456-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,4,5 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 163456-99:
(8*1)+(7*6)+(6*3)+(5*4)+(4*5)+(3*6)+(2*9)+(1*9)=153
153 % 10 = 3
So 163456-99-3 is a valid CAS Registry Number.

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163456-99-3Relevant academic research and scientific papers

Cycloaddition Reactions of Carbohydrate Derivatives. Part VI. Quinolizidine Analogs of Castanospermine

Herczegh, Pal,Kovacs, Imre,Szilagyi, Laszlo,Sztaricskai, Ferenc,Berecibar, Amaya,et al.

, p. 2969 - 2978 (2007/10/02)

Octahydroquinolizine-1,2,3,8-tetraols 12, 16 and 23, analogs of castanospermine, were synthesized from D-glucose, L-arabinose and D-mannose, respectively, using hetero-Diels-Alder reactions of sugar-derived azomethines as the key step.

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