Cas 81027-62-5,(13S,14R,17S)-15-Methoxy-16,17-diphenyl-11,12,13,14-tetrahydro-17-phospha-cyclopenta[a]phenanthrene 17-oxide

81027-62-5

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Basic information

Product Name: (13S,14R,17S)-15-Methoxy-16,17-diphenyl-11,12,13,14-tetrahydro-17-phospha-cyclopenta[a]phenanthrene 17-oxide
Synonyms:
CAS NO:81027-62-5
Molecular Formula:
Molecular Weight: 436.49
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: (13S,14R,17S)-15-Methoxy-16,17-diphenyl-11,12,13,14-tetrahydro-17-phospha-cyclopenta[a]phenanthrene 17-oxide(CAS DataBase Reference)
NIST Chemistry Reference: (13S,14R,17S)-15-Methoxy-16,17-diphenyl-11,12,13,14-tetrahydro-17-phospha-cyclopenta[a]phenanthrene 17-oxide(81027-62-5)
EPA Substance Registry System: (13S,14R,17S)-15-Methoxy-16,17-diphenyl-11,12,13,14-tetrahydro-17-phospha-cyclopenta[a]phenanthrene 17-oxide(81027-62-5)

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: 81027-62-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81027-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,2 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81027-62:
(7*8)+(6*1)+(5*0)+(4*2)+(3*7)+(2*6)+(1*2)=105
105 % 10 = 5
So 81027-62-5 is a valid CAS Registry Number.

81027-62-5Upstream product

81027-62-5Downstream Products

81027-62-5Relevant academic research and scientific papers

An Efficient Synthesis of the Enantiomeric 17-Phosphasteroid System

Bodalski, Ryszard,Koszuk, Jacek,Krawczyk, Henryk,Pietrusiewicz, K. Michal

, p. 2219 - 2220 (2007/10/02)

Enantiomeric trans-benzylphenylphosphine oxide (6) undergoes regio- and stereoselective cycloaddition to 1-vinylnaphthalene (5), providing two diastereomeric adducts 7a and 7b, which are further transformed into optically pure 17-phosphasteroid systems by intramolecular Dieckmann-type condensation.

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