Cas 945867-31-2,trans-3β-acetoxy-16,17-secopregna-5,17(20)-dien-16-al (E)-4'-(trifluoromethyl)phenylhydrazone

945867-31-2

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Basic information

Product Name: trans-3β-acetoxy-16,17-secopregna-5,17(20)-dien-16-al (E)-4'-(trifluoromethyl)phenylhydrazone
Synonyms: trans-3β-acetoxy-16,17-secopregna-5,17(20)-dien-16-al (E)-4'-(trifluoromethyl)phenylhydrazone
CAS NO:945867-31-2
Molecular Formula:
Molecular Weight: 516.647
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: trans-3β-acetoxy-16,17-secopregna-5,17(20)-dien-16-al (E)-4'-(trifluoromethyl)phenylhydrazone(CAS DataBase Reference)
NIST Chemistry Reference: trans-3β-acetoxy-16,17-secopregna-5,17(20)-dien-16-al (E)-4'-(trifluoromethyl)phenylhydrazone(945867-31-2)
EPA Substance Registry System: trans-3β-acetoxy-16,17-secopregna-5,17(20)-dien-16-al (E)-4'-(trifluoromethyl)phenylhydrazone(945867-31-2)

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: 945867-31-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945867-31-2 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 945867-31:
(8*9)+(7*4)+(6*5)+(5*8)+(4*6)+(3*7)+(2*3)+(1*1)=222
222 % 10 = 2
So 945867-31-2 is a valid CAS Registry Number.

945867-31-2Upstream product

945867-31-2Downstream Products

945867-31-2Relevant academic research and scientific papers

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

, p. 3894 - 3904 (2009)

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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