17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

Base Information

Chemical Name:17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane
CAS No.:225245-12-5
Molecular Formula:C₃₂H₅₂O₂Si
Molecular Weight:496.849
Hs Code.:

Synonyms:17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

Suppliers and Price of 17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

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

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Chemical Property of 17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

Chemical Property:

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Technology Process of 17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

There total 6 articles about 17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane 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:

: 521-18-6
Stanolone

: 225245-12-5
17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / imidazole / dimethylformamide / 20 °C

2: tetrahydrofuran / 0 - 20 °C

With 1H-imidazole; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm058179h

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 225245-12-5
17β-[(tert-butyldimethylsilyl)oxy]-3α-hydroxy-3β-phenylmethyl-5α-androstane

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / imidazole / dimethylformamide / 20 °C

2: tetrahydrofuran / 0 - 20 °C

With 1H-imidazole; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm058179h