Cas 728003-58-5,(3S,5aR,6R,7S,8aR)-7-Methyl-6-nitromethyl-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one

728003-58-5

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Basic information

Product Name: (3S,5aR,6R,7S,8aR)-7-Methyl-6-nitromethyl-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one
Synonyms: (3S,5aR,6R,7S,8aR)-7-Methyl-6-nitromethyl-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one
CAS NO:728003-58-5
Molecular Formula:
Molecular Weight: 316.357
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: (3S,5aR,6R,7S,8aR)-7-Methyl-6-nitromethyl-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5aR,6R,7S,8aR)-7-Methyl-6-nitromethyl-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one(728003-58-5)
EPA Substance Registry System: (3S,5aR,6R,7S,8aR)-7-Methyl-6-nitromethyl-3-phenyl-hexahydro-1-oxa-3a-aza-cyclopenta[c]pentalen-4-one(728003-58-5)

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: 728003-58-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 728003-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,0,0 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 728003-58:
(8*7)+(7*2)+(6*8)+(5*0)+(4*0)+(3*3)+(2*5)+(1*8)=145
145 % 10 = 5
So 728003-58-5 is a valid CAS Registry Number.

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728003-58-5Relevant academic research and scientific papers

A simple reaction to produce small structurally complex and diverse molecules

Deprez-Poulain, Rebecca,Willand, Nicolas,Boutillon, Christophe,Nowogrocki, Guy,Azaroual, Nathalie,Deprez, Benoit

, p. 5287 - 5290 (2004)

In order to mimic the complexity of natural products, we designed and obtained with simple synthetic methods, building blocks with 'quaternary chiral centers'. These tricyclic lactams resulted from the reaction of a functional γ-keto-acid and various comm

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