Cas 158146-79-3,(-)-(1S,6R,6aS,7R)-6-(Benzoyloxy)-7-carbomethoxy-1-<(phenoxythiocarbonyl)oxy>hexahydro-1H-pyrrolizin-2-one

158146-79-3

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Basic information

Product Name: (-)-(1S,6R,6aS,7R)-6-(Benzoyloxy)-7-carbomethoxy-1-<(phenoxythiocarbonyl)oxy>hexahydro-1H-pyrrolizin-2-one
Synonyms: (-)-(1S,6R,6aS,7R)-6-(Benzoyloxy)-7-carbomethoxy-1-<(phenoxythiocarbonyl)oxy>hexahydro-1H-pyrrolizin-2-one
CAS NO:158146-79-3
Molecular Formula:
Molecular Weight: 455.488
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: (-)-(1S,6R,6aS,7R)-6-(Benzoyloxy)-7-carbomethoxy-1-<(phenoxythiocarbonyl)oxy>hexahydro-1H-pyrrolizin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(1S,6R,6aS,7R)-6-(Benzoyloxy)-7-carbomethoxy-1-<(phenoxythiocarbonyl)oxy>hexahydro-1H-pyrrolizin-2-one(158146-79-3)
EPA Substance Registry System: (-)-(1S,6R,6aS,7R)-6-(Benzoyloxy)-7-carbomethoxy-1-<(phenoxythiocarbonyl)oxy>hexahydro-1H-pyrrolizin-2-one(158146-79-3)

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: 158146-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 158146-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,1,4 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 158146-79:
(8*1)+(7*5)+(6*8)+(5*1)+(4*4)+(3*6)+(2*7)+(1*9)=153
153 % 10 = 3
So 158146-79-3 is a valid CAS Registry Number.

158146-79-3Upstream product

1005-56-7 phenylcarbonochloridothioate

158146-79-3Downstream Products

158146-79-3Relevant academic research and scientific papers

The tandem cycloaddition chemistry of nitroalkenes. A novel synthesis of (-)-hastanecine

Denmark,Thorarensen

, p. 5672 - 5680 (1994)

A short and efficient asymmetric synthesis of the pyrrolizidine necine base (-)-hastanecine is described. The key reaction in the synthesis is a sequential inter [4 + 2]/inter [3 + 2] cycloaddition. The Lewis acid promoted [4 + 2] cycloaddition between 2-

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