Cas 1534363-84-2,2-((8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14, 15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carbonyl)-3-phenylacrylonitrile

1534363-84-2

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Basic information

Product Name: 2-((8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14, 15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carbonyl)-3-phenylacrylonitrile
Synonyms:
CAS NO:1534363-84-2
Molecular Formula:
Molecular Weight: 427.587
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: 2-((8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14, 15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carbonyl)-3-phenylacrylonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-((8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14, 15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carbonyl)-3-phenylacrylonitrile(1534363-84-2)
EPA Substance Registry System: 2-((8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14, 15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-17-carbonyl)-3-phenylacrylonitrile(1534363-84-2)

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: 1534363-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1534363-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,4,3,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1534363-84:
(9*1)+(8*5)+(7*3)+(6*4)+(5*3)+(4*6)+(3*3)+(2*8)+(1*4)=162
162 % 10 = 2
So 1534363-84-2 is a valid CAS Registry Number.

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1534363-84-2Relevant academic research and scientific papers

Synthesis of progesterone derivatives and evaluation of their efficiency as pneumococcal vaccines

Mohareb, Rafat M.,Al Farouk, Fatma O.,Sherif, Sherif M.,Karaghiosoff, Konstantin

, p. 3165 - 3177 (2014/05/06)

Progesterone (1) was used as a template to develop new anticancer compounds. Ring D modification of 1, through its reaction with active methylene derivatives, gave the condensate derivatives 3a, b. The latter compounds underwent heterocyclization reaction

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