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Cas Database

Name	1-Testosterone	EINECS	200-533-0
CAS No.	65-06-5	Density	1.1561
PSA	37.30000	LogP	3.73510
Solubility	N/A	Melting Point	75-85°C
Formula	C19H28 O2	Boiling Point	120°C 0,5mm
Molecular Weight	288.43	Flash Point	179.5oC
Transport Information	N/A	Appearance	N/A
Safety		Risk Codes	N/A
Molecular Structure		Hazard Symbols	Xi
Synonyms	5a-Androst-1-en-3-one, 17b-hydroxy- (8CI);1-Testosterone;17b-Hydroxy-5a-androst-1-en-3-one;5a-Androst-1-en-17b-ol-3-one;NSC 121140;NSC 39366;	Article Data	18

1-Testosterone Synthetic route

: 64-82-4, 6656-41-3, 21507-42-6, 25615-33-2, 54631-35-5, 79732-37-9, 97413-69-9
(5α,17β)-3-oxoandrost-1-en-17-yl acetate

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
With sodium hydroxide In methanol at 20℃; for 2h;	99.8%

: 1971-67-1
5α-androst-1-en-3-one-17β-yl benzoate

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
With sodium hydroxide for 2h; Heating;	82.6%

: 119572-14-4
17β-cyclohexanecarbonyloxy-5α-androst-1-en-3-one

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
With potassium hydroxide

: 38859-38-0
5α-androst-1-ene-3α,17β-diol

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
With manganese(IV) oxide In dichloromethane

: 63109-26-2
2-((3S,5S,8R,9S,10R,13S,14S,17S)-3,17-Dihydroxy-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-yl)-N,N-dimethyl-acetamide

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
at 250℃;

17β-acetoxy-5α-androsten-(1)-one-(3): 17β-acetoxy-5α-androsten-(1)-one-(3)

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
With potassium hydroxide

: 952222-37-6
17β-acetoxy-2-bromo-5α-androstan-3-one

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 99.6 percent / lithium bromide; lithium carbonate / dimethylformamide / 0.5 h / Heating 2: 99.8 percent / sodium hydroxide / methanol / 2 h / 20 °C View Scheme

: 1164-91-6
stanolone acetate

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 88 percent / hydrogen chloride; bromine / acetic acid / 1 h / 20 - 25 °C 2: 99.6 percent / lithium bromide; lithium carbonate / dimethylformamide / 0.5 h / Heating 3: 99.8 percent / sodium hydroxide / methanol / 2 h / 20 °C View Scheme

: 1057-07-4
stanolone benzoate

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 5.1 g / Br2 / acetic acid / 3 h / Ambient temperature 2: CaCO3 / N,N-dimethyl-acetamide / 0.33 h / Heating 3: 82.6 percent / 5percent methanolic NaOH / 2 h / Heating View Scheme

: 96192-10-8
2α-Brom-17β-benzoyloxy-5α-androstanon-(3)

: 65-06-5
1-testosterone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: CaCO3 / N,N-dimethyl-acetamide / 0.33 h / Heating 2: 82.6 percent / 5percent methanolic NaOH / 2 h / Heating View Scheme

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