Cas 128164-66-9,(3aS,6aR)-2-Ethyl-6a-(3-oxo-3-phenyl-propionyl)-hexahydro-cyclopenta[c]pyrrole-3a-carboxylic acid ethyl ester

128164-66-9

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Basic information

Product Name: (3aS,6aR)-2-Ethyl-6a-(3-oxo-3-phenyl-propionyl)-hexahydro-cyclopenta[c]pyrrole-3a-carboxylic acid ethyl ester
Synonyms:
CAS NO:128164-66-9
Molecular Formula:
Molecular Weight: 357.45
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: (3aS,6aR)-2-Ethyl-6a-(3-oxo-3-phenyl-propionyl)-hexahydro-cyclopenta[c]pyrrole-3a-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,6aR)-2-Ethyl-6a-(3-oxo-3-phenyl-propionyl)-hexahydro-cyclopenta[c]pyrrole-3a-carboxylic acid ethyl ester(128164-66-9)
EPA Substance Registry System: (3aS,6aR)-2-Ethyl-6a-(3-oxo-3-phenyl-propionyl)-hexahydro-cyclopenta[c]pyrrole-3a-carboxylic acid ethyl ester(128164-66-9)

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: 128164-66-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128164-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128164-66:
(8*1)+(7*2)+(6*8)+(5*1)+(4*6)+(3*4)+(2*6)+(1*6)=129
129 % 10 = 9
So 128164-66-9 is a valid CAS Registry Number.

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128164-66-9Relevant academic research and scientific papers

Reactions of Bridgehead Halides. A Synthesis of Modhephene, Isomodhephene, and epi-Modhephene

Kraus, George A.,Shi, Jianmin

, p. 4147 - 4151 (1991)

A synthesis of modhephene has been achieved, the key feature of which is the use of a novel nucleophilic addition/rearrangement reaction to develop the carbon framework.Stereochemical control of the stereogenic center bearing the methyl group was accompli

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