(8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene

Base Information

Chemical Name:(8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene
CAS No.:28805-72-3
Molecular Formula:C₁₉H₃₂
Molecular Weight:260.463
Hs Code.:
Mol file:28805-72-3.mol

Synonyms:(8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene

Suppliers and Price of (8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene

Chemical Property:

Vapor Pressure:0.000224mmHg at 25°C
Boiling Point:336°C at 760 mmHg
Flash Point:145.9°C
Density:0.95g/cm³

Purity/Quality:

Safty Information:

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Hazard Codes:

MSDS Files:

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Technology Process of (8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene

There total 45 articles about (8S-(8alpha,9beta,10alpha,13alpha,14beta))-Hexadecahydro-10,13-dimethy l-1H-cyclopenta(a)phenanthrene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

: 26313-26-8
17-iodo-5α-androst-16-ene

: 762-04-9
phosphonic acid diethyl ester

: 438-22-2,28805-72-3
(5α)-androstane

: 6618-43-5
Δ¹⁶-androstene

: diethyl androst-16-ene-17-phosphonate

Guidance literature:: With triethylamine; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; at 110 ℃; for 20h;
DOI:10.1016/0039-128X(95)00121-6

Reference yield: 83.0%

: 1809-20-7
diisopropyl hydrogenphosphonate

: 26313-26-8
17-iodo-5α-androst-16-ene

: 438-22-2,28805-72-3
(5α)-androstane

: 6618-43-5
Δ¹⁶-androstene

: diisopropyl androst-16-ene-17-phosphonate

Guidance literature:: With triethylamine; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; at 110 ℃; for 20h; Product distribution; Mechanism; var. of catalyst, amine, ratio, temp., time, further in solvents;
DOI:10.1016/0039-128X(95)00121-6