Cas 1241046-56-9,16E-(4-difluoromethoxy-3-methoxybenzylidene)-3β-hydroxy-androst-5-en-17-one

1241046-56-9

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Basic information

Product Name: 16E-(4-difluoromethoxy-3-methoxybenzylidene)-3β-hydroxy-androst-5-en-17-one
Synonyms: 16E-(4-difluoromethoxy-3-methoxybenzylidene)-3β-hydroxy-androst-5-en-17-one
CAS NO:1241046-56-9
Molecular Formula:
Molecular Weight: 472.572
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: 16E-(4-difluoromethoxy-3-methoxybenzylidene)-3β-hydroxy-androst-5-en-17-one(CAS DataBase Reference)
NIST Chemistry Reference: 16E-(4-difluoromethoxy-3-methoxybenzylidene)-3β-hydroxy-androst-5-en-17-one(1241046-56-9)
EPA Substance Registry System: 16E-(4-difluoromethoxy-3-methoxybenzylidene)-3β-hydroxy-androst-5-en-17-one(1241046-56-9)

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: 1241046-56-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1241046-56-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,0,4 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1241046-56:
(9*1)+(8*2)+(7*4)+(6*1)+(5*0)+(4*4)+(3*6)+(2*5)+(1*6)=109
109 % 10 = 9
So 1241046-56-9 is a valid CAS Registry Number.

1241046-56-9Upstream product

1241046-56-9Downstream Products

1241046-63-8 3β-acetoxy-16E-(4-difluoromethoxy-3-methoxybenzylidene)-androst-5-en-17-one

1241046-56-9Relevant academic research and scientific papers

New steroid α, β-unsaturated ketones as chiral components of induced cholesteric liquid crystal systems

Yaremenko,Pivnenko,Kutulya,Kondratyuk,Novikova,Shkolnikova

, p. 1072 - 1083 (2009)

New (E)-16-arylidene derivatives of 3β-hydroxyandrost-5-en-17-one and their acetates containing different substituents in the arylidene fragment were synthesized. The ability of the synthesized chiral compounds to induce helical supramolecular ordering (t

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