Cas 4659-60-3,13-ethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl decanoate (non-preferred name)

4659-60-3

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Basic information

Product Name: 13-ethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl decanoate (non-preferred name)
Synonyms:
CAS NO:4659-60-3
Molecular Formula: C₂₉H₄₆O₃
Molecular Weight: 442.6737
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 548.7°C at 760 mmHg
Flash Point: 230.7°C
Appearance: N/A
Density: 1.04g/cm³
Vapor Pressure: 4.31E-12mmHg at 25°C
Refractive Index: 1.523
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 13-ethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl decanoate (non-preferred name)(CAS DataBase Reference)
NIST Chemistry Reference: 13-ethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl decanoate (non-preferred name)(4659-60-3)
EPA Substance Registry System: 13-ethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl decanoate (non-preferred name)(4659-60-3)

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: 4659-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 4659-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4659-60:
(6*4)+(5*6)+(4*5)+(3*9)+(2*6)+(1*0)=113
113 % 10 = 3
So 4659-60-3 is a valid CAS Registry Number.

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4659-60-3Relevant academic research and scientific papers

Synthesis of 13-alkyl-gon-4-ones

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, (2008/06/13)

The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

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