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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
ChemicalBook CAS DataBase List 17-Methyltestosterone

17-Methyltestosterone synthesis

10synthesis methods
Methyltestosterone, 17β-hydroxy-17α-methylandrost-4-en-3-one (29.1.7), is also synthesized from androstenolone by reacting it with methylmagnesiumiodide, forming the corresponding tertiary alcohol (29.1.6), and subsequent oxidation of the hydroxyl group at C3 to a ketone using chromium (VI) oxide. Simultaneous isomerization of the double bond takes place under the reaction conditions, giving the desired methyltestosterone (29.1.7).

3-hydroxypregna-5,16-dien-20-one 3-acetate

38521-84-5
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17-Methyltestosterone

58-18-4
307 suppliers
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Yield:-

Steps:

Multi-step reaction with 4 steps
1: hydroxylamine hydrochloride
2: pyridine; trichlorophosphate / N,N-dimethyl-formamide
3: sodium hydroxide; sodium tetrahydroborate
4: manganese(IV) oxide

References:

CN106397521,2017,A

Methandriol

521-10-8
42 suppliers
$60.00/500mg

17-Methyltestosterone

58-18-4
307 suppliers
$33.00/1mg

References
Androst-4-en-3-one, 17-methyl-17-[(tetrahydro-2-furanyl)oxy]-, (17β)- (9CI)

111222-36-7
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17-Methyltestosterone

58-18-4
307 suppliers
$33.00/1mg

References
72-63-9 Synthesis
Metandienone

72-63-9
318 suppliers
$28.00/1mg

17-Methyltestosterone

58-18-4
307 suppliers
$33.00/1mg

References
57-83-0 Synthesis
Progesterone

57-83-0
798 suppliers
$17.00/1g

16-Dehydroprogesterone

1096-38-4
108 suppliers
$50.00/50mg

17-Methyltestosterone

58-18-4
307 suppliers
$33.00/1mg

145-13-1 Synthesis
Pregnenolone

145-13-1
485 suppliers
$28.00/500mg

64-85-7 Synthesis
Desoxycorticosterone

64-85-7
127 suppliers
$15.00/5mg

Pregna-4,7-diene-3,20-dione

17398-60-6
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Pregna-3,6,20-trione

30802-24-5
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3,20-allopregnanedione

7350-00-7
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References

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