Cas 6015-78-7,(8R,9S,13S,14S)-13-Methyl-3-(2-phenyl-quinazolin-4-yloxy)-6,7,8,9,11,12,13,14,15,16-decahydro-cyclopenta[a]phenanthren-17-one

6015-78-7

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Basic information

Product Name: (8R,9S,13S,14S)-13-Methyl-3-(2-phenyl-quinazolin-4-yloxy)-6,7,8,9,11,12,13,14,15,16-decahydro-cyclopenta[a]phenanthren-17-one
Synonyms: (8R,9S,13S,14S)-13-Methyl-3-(2-phenyl-quinazolin-4-yloxy)-6,7,8,9,11,12,13,14,15,16-decahydro-cyclopenta[a]phenanthren-17-one
CAS NO:6015-78-7
Molecular Formula:
Molecular Weight: 474.602
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: (8R,9S,13S,14S)-13-Methyl-3-(2-phenyl-quinazolin-4-yloxy)-6,7,8,9,11,12,13,14,15,16-decahydro-cyclopenta[a]phenanthren-17-one(CAS DataBase Reference)
NIST Chemistry Reference: (8R,9S,13S,14S)-13-Methyl-3-(2-phenyl-quinazolin-4-yloxy)-6,7,8,9,11,12,13,14,15,16-decahydro-cyclopenta[a]phenanthren-17-one(6015-78-7)
EPA Substance Registry System: (8R,9S,13S,14S)-13-Methyl-3-(2-phenyl-quinazolin-4-yloxy)-6,7,8,9,11,12,13,14,15,16-decahydro-cyclopenta[a]phenanthren-17-one(6015-78-7)

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: 6015-78-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6015-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6015-78:
(6*6)+(5*0)+(4*1)+(3*5)+(2*7)+(1*8)=77
77 % 10 = 7
So 6015-78-7 is a valid CAS Registry Number.

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6015-78-7Relevant academic research and scientific papers

New efficient pathway for the synthesis of 3-aminoestrone

Radu, Ioan-Iosif,Poirier, Donald,Provencher, Louis

, p. 7617 - 7619 (2002)

3-Aminoestrone, a non-natural C-18 steroid, was synthesized by the classical and by a new efficient pathway, the latter using benzophenone imine as an ammonia equivalent in the palladium(0)-catalysed amination of estrone-triflate. This methodology circumv

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