Cas 155936-54-2,(1S,7aR)-3-Methyl-1-((1S,2R)-2-phenyl-cyclohexyloxy)-1,4,5,6,7,7a-hexahydro-inden-2-one

155936-54-2

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Basic information

Product Name: (1S,7aR)-3-Methyl-1-((1S,2R)-2-phenyl-cyclohexyloxy)-1,4,5,6,7,7a-hexahydro-inden-2-one
Synonyms:
CAS NO:155936-54-2
Molecular Formula:
Molecular Weight: 324.463
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,7aR)-3-Methyl-1-((1S,2R)-2-phenyl-cyclohexyloxy)-1,4,5,6,7,7a-hexahydro-inden-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,7aR)-3-Methyl-1-((1S,2R)-2-phenyl-cyclohexyloxy)-1,4,5,6,7,7a-hexahydro-inden-2-one(155936-54-2)
EPA Substance Registry System: (1S,7aR)-3-Methyl-1-((1S,2R)-2-phenyl-cyclohexyloxy)-1,4,5,6,7,7a-hexahydro-inden-2-one(155936-54-2)

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: 155936-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155936-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,3 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 155936-54:
(8*1)+(7*5)+(6*5)+(5*9)+(4*3)+(3*6)+(2*5)+(1*4)=162
162 % 10 = 2
So 155936-54-2 is a valid CAS Registry Number.

155936-54-2Upstream product

155936-54-2Downstream Products

155936-55-3 (1S,3S,3aR,7aR)-1-Methyl-3-((1S,2R)-2-phenyl-cyclohexyloxy)-octahydro-inden-2-one

155936-54-2Relevant academic research and scientific papers

Asymmetric synthesis of bicyclo[4.3.0]nonan-8-ones by intramolecular Pauson-Khand reaction

Castro,Moyano,Pericas,Riera,Greene

, p. 307 - 310 (2007/10/02)

The intramolecular Pauson-Khand reaction of (E)-1-alkoxy-1-octen-7-ynes derived from (1S,2R)-2-phenylcyclohexanol is described. 7-Alkoxybicyclo[4.3.0]non-1(9)-en-8-ones are obtained in yields up to 65% and with diastereoselectivities higher than 10:1. The

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