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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
641-82-7

17b-Methyl-5a-androstane-3a,17b-diol synthesis

5synthesis methods
521-11-9 Synthesis
Mestanolone

521-11-9
224 suppliers
$120.00/0.500g

17b-Methyl-5a-androstane-3a,17b-diol

641-82-7
12 suppliers
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-

Yield:641-82-7 267 mg

Reaction Conditions:

with potassium tri-sec-butyl-borohydride in tetrahydrofuran at -78;

References:

Templeton;Choi Jackson [Steroids,1983,vol. 41,# 4,p. 485 - 491]

(5S,8S,9S,10S,13S,14S,17S)-10,13,17-trimethyl-1,4,5,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ol

3275-64-7
17 suppliers
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17b-Methyl-5a-androstane-3a,17b-diol

641-82-7
12 suppliers
inquiry

References
917-64-6 Synthesis
METHYLMAGNESIUM IODIDE

917-64-6
147 suppliers
$45.00/10ml

Androstan-16-one, 3-hydroxy-, (3α,5α)-

27741-16-8
0 suppliers
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17b-Methyl-5a-androstane-3a,17b-diol

641-82-7
12 suppliers
inquiry

References
Androsterone

53-41-8
213 suppliers
$28.60/1MG

Methylmagnesium Bromide

75-16-1
276 suppliers
$12.00/10ml

17b-Methyl-5a-androstane-3a,17b-diol

641-82-7
12 suppliers
inquiry

References
917-64-6 Synthesis
METHYLMAGNESIUM IODIDE

917-64-6
147 suppliers
$45.00/10ml

Diethyl ether

60-29-7
0 suppliers
$31.19/50g

Androsterone

53-41-8
213 suppliers
$28.60/1MG

17b-Methyl-5a-androstane-3a,17b-diol

641-82-7
12 suppliers
inquiry

References

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