Cas 140835-51-4,5-carbomethoxy-2,2aα,3,4,4aα,5β,6α,7α,7aα,7bα-decahydro-1,7b-dimethyl-4a-hydroxy-6-(1-methylethyl)-1H-cyclopent<cd>indol-7-yl 4-phenylbenzoate

140835-51-4

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Basic information

Product Name: 5-carbomethoxy-2,2aα,3,4,4aα,5β,6α,7α,7aα,7bα-decahydro-1,7b-dimethyl-4a-hydroxy-6-(1-methylethyl)-1H-cyclopentindol-7-yl 4-phenylbenzoate
Synonyms: 5-carbomethoxy-2,2aα,3,4,4aα,5β,6α,7α,7aα,7bα-decahydro-1,7b-dimethyl-4a-hydroxy-6-(1-methylethyl)-1H-cyclopentindol-7-yl 4-phenylbenzoate
CAS NO:140835-51-4
Molecular Formula:
Molecular Weight: 491.627
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: 5-carbomethoxy-2,2aα,3,4,4aα,5β,6α,7α,7aα,7bα-decahydro-1,7b-dimethyl-4a-hydroxy-6-(1-methylethyl)-1H-cyclopentindol-7-yl 4-phenylbenzoate(CAS DataBase Reference)
NIST Chemistry Reference: 5-carbomethoxy-2,2aα,3,4,4aα,5β,6α,7α,7aα,7bα-decahydro-1,7b-dimethyl-4a-hydroxy-6-(1-methylethyl)-1H-cyclopentindol-7-yl 4-phenylbenzoate(140835-51-4)
EPA Substance Registry System: 5-carbomethoxy-2,2aα,3,4,4aα,5β,6α,7α,7aα,7bα-decahydro-1,7b-dimethyl-4a-hydroxy-6-(1-methylethyl)-1H-cyclopentindol-7-yl 4-phenylbenzoate(140835-51-4)

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: 140835-51-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140835-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 140835-51:
(8*1)+(7*4)+(6*0)+(5*8)+(4*3)+(3*5)+(2*5)+(1*1)=114
114 % 10 = 4
So 140835-51-4 is a valid CAS Registry Number.

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140835-51-4Relevant academic research and scientific papers

Acylnitrilium ion initiated heteroannulations in alkaloid synthesis. An efficient, stereocontrolled, total synthesis of the Orchidaceae alkaloid (±)-dendrobine

Lee, Cheol Hae,Westling, Mark,Livinghouse, Tom,Williams, Andrew C.

, p. 4089 - 4095 (1992)

A concise total synthesis of (±)-dendrobine is described that proceeds in eight steps from 2-methylcyclopent-2-en-1-one. The key transformation in this approach is the silver ion mediated cyclocondensation of the isonitrile 6 with the acyl chloride 5. Thi

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