Cas 945867-36-7,(3'S,17S)-3'-methyl-2'-(4-trifluoromethylphenyl)-3',4'-dihydro-2'H-pyrazolo[4',5':17,16]androst-5-ene 3β-acetate

945867-36-7

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Basic information

Product Name: (3'S,17S)-3'-methyl-2'-(4-trifluoromethylphenyl)-3',4'-dihydro-2'H-pyrazolo[4',5':17,16]androst-5-ene 3β-acetate
Synonyms: (3'S,17S)-3'-methyl-2'-(4-trifluoromethylphenyl)-3',4'-dihydro-2'H-pyrazolo[4',5':17,16]androst-5-ene 3β-acetate
CAS NO:945867-36-7
Molecular Formula:
Molecular Weight: 514.631
EINECS: N/A
Product Categories: N/A
Mol File: 945867-36-7.mol
Article Data: 2

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: (3'S,17S)-3'-methyl-2'-(4-trifluoromethylphenyl)-3',4'-dihydro-2'H-pyrazolo[4',5':17,16]androst-5-ene 3β-acetate(CAS DataBase Reference)
NIST Chemistry Reference: (3'S,17S)-3'-methyl-2'-(4-trifluoromethylphenyl)-3',4'-dihydro-2'H-pyrazolo[4',5':17,16]androst-5-ene 3β-acetate(945867-36-7)
EPA Substance Registry System: (3'S,17S)-3'-methyl-2'-(4-trifluoromethylphenyl)-3',4'-dihydro-2'H-pyrazolo[4',5':17,16]androst-5-ene 3β-acetate(945867-36-7)

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: 945867-36-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945867-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,8,6 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 945867-36:
(8*9)+(7*4)+(6*5)+(5*8)+(4*6)+(3*7)+(2*3)+(1*6)=227
227 % 10 = 7
So 945867-36-7 is a valid CAS Registry Number.

945867-36-7Upstream product

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945867-36-7Relevant articles and documents

Efficient approach to androstene-fused arylpyrazolines as potent antiproliferative agents. Experimental and theoretical studies of substituent effects on BF3-catalyzed intramolecular [3 + 2] cycloadditions of olefinic phenylhydrazones

Frank, Eva,Mucsi, Zoltan,Zupkd, Istvan,Rethy, Borbala,Falkay, George,Schneider, Gyula,Woelfling, Janos

supporting information; experimental part, p. 3894 - 3904 (2009/08/08)

Highly diastereoselective Lewis acid induced intramolecular 1,3-dipolar cycloadditions of alkenyl phenylhydrazones (containing various substituents on the aromatic ring) obtained from a D-secopregnene aldehyde were carried out under fairly mild conditions

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