Cas 75336-40-2,(4S,5R,6R,7R)-4,5,6,7,8-Pentaacetoxy-2-[1-benzylamino-eth-(Z)-ylidene]-3-nitromethyl-octanoic acid methyl ester

75336-40-2

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Basic information

Product Name: (4S,5R,6R,7R)-4,5,6,7,8-Pentaacetoxy-2-[1-benzylamino-eth-(Z)-ylidene]-3-nitromethyl-octanoic acid methyl ester
Synonyms:
CAS NO:75336-40-2
Molecular Formula:
Molecular Weight: 638.626
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: (4S,5R,6R,7R)-4,5,6,7,8-Pentaacetoxy-2-[1-benzylamino-eth-(Z)-ylidene]-3-nitromethyl-octanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R,6R,7R)-4,5,6,7,8-Pentaacetoxy-2-[1-benzylamino-eth-(Z)-ylidene]-3-nitromethyl-octanoic acid methyl ester(75336-40-2)
EPA Substance Registry System: (4S,5R,6R,7R)-4,5,6,7,8-Pentaacetoxy-2-[1-benzylamino-eth-(Z)-ylidene]-3-nitromethyl-octanoic acid methyl ester(75336-40-2)

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: 75336-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75336-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75336-40:
(7*7)+(6*5)+(5*3)+(4*3)+(3*6)+(2*4)+(1*0)=132
132 % 10 = 2
So 75336-40-2 is a valid CAS Registry Number.

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75336-40-2Relevant academic research and scientific papers

Synthesis of 3-(Polyacetoxyalkyl)pyrroles from 3-Aminocrotonic Esters and Open-chain Sugar Nitro-olefins

Gomez-Sanchez, Antonio,Mancera, Manuel,Rosado, Francisco,Bellanato, Juana

, p. 1199 - 1205 (2007/10/02)

D-gluco- and D-galacto-3,4,5,6,7-Penta-acetoxy-1-nitrohept-1-ene (1a and b) reacted with 3-(alkylamino)crotonic esters (2) yielding the Michael-type adducts (3) which have a preference for the intramolecularly bonded (Z)-configuration.These compounds were

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