CasNo：2363-59-9
Product Name:Boldenone Acetate
Molecular Formula:C21H28O3
Purity:99%
High Purity 99% Buy High Grade Boldenone Acetate 2363-59-9 In Bulk Supply
- Molecular Formula:C21H28O3
- Molecular Weight:328.452
- Vapor Pressure:4.58E-08mmHg at 25°C
- Melting Point:149-151 °C
- Refractive Index:1.555
- Boiling Point:443.6 °C at 760 mmHg
- Flash Point:192.7 °C
- PSA：43.37000
- Density:1.13 g/cm3
- LogP:4.22600
Boldenone 17-acetate(Cas 2363-59-9) Usage
|
Description |
Boldenone 17-acetate is a white or white solid powder, belongs to the hormone class. |
|
Uses |
The parent of 17-acetate bodanone is a derivative of testosterone and thus inherits most of its properties, such as androgenic ability and protein synthesis. |
InChI:InChI=1/C21H28O3/c1-13(22)24-19-7-6-17-16-5-4-14-12-15(23)8-10-20(14,2)18(16)9-11-21(17,19)3/h8,10,12,16-19H,4-7,9,11H2,1-3H3
2363-59-9 Relevant articles
STEROID HOMOLOG CONTAINING A PYRAZOLE NUCLEUS.
VIDA,GUT
, p. 792 - 793 (1963)
-
Use of [1,2-3H] Testosterone in 5- Reductase Enzymatic Activity Dosing in Dermal Fibroblast Cultures from Polycystic Ovarian Patients
Matei, L.,Postolache, C.,Fugaru, V.,Condac, E.,Dinichiotu, A.,Costache, M.
, p. 1055 - 1056 (2007/10/03)
-
2-iodo-3-keto-Δ4 steroids, process for their production, as well as their further processing
-
, (2008/06/13)
The new intermediate products of general...
2363-59-9 Process route
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1045-69-8
testosterone acetate
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2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one
| Conditions | Yield |
|---|---|
|
With
thallium(III) acetate;
In
acetic acid;
|
|
|
With
2,6-dichloro-3,5-dicyano-1,4-benzoquinone;
|
-
![Acetic acid (8R,9S,10R,13S,14S,17S)-6-bromo-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl ester](/upload/2023/8/b61745a2-9ebf-4419-854b-14bc45fecaf1.png)
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Acetic acid (8R,9S,10R,13S,14S,17S)-6-bromo-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl ester
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-
2363-59-9
17β-acetoxy-androsta-1,4-dien-3-one
| Conditions | Yield |
|---|---|
|
Multi-step reaction with 2 steps
1: Zn / aq. ethanol
2: (i) (UV-irradiation), EtOH, (ii) KOH, MeOH, (iii) /BRN= 385737/, Py
With
zinc;
In
ethanol;
|
2363-59-9 Upstream products
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108-75-8
2,4,6-trimethyl-pyridine
-
82926-51-0
17β-acetoxy-2β,4β-dibromo-5β-androstan-3-one
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15359-18-9
17β-Acetoxy-3-oxo-Δ1,5-androstadien
-
108-24-7
acetic anhydride
2363-59-9 Downstream products
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2456-11-3
1-Methyl-17-o-acetyl-oestradiol
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2383-80-4
(1Ξ,6Ξ,3'aS)-6't-acetoxy-4,5'a-dimethyl-(3'ar,5'at,8'ac,8'bt)-decahydro-spiro[bicyclo[3.1.0]hex-3-ene-6,3'-As-indacen]-2-one
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2363-60-2
17β-acetoxy-1β,5β-cyclo-10α-androst-3-en-2-one
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2363-60-2
2-Oxo-17β-acetoxy-1α.5β-cyclo-Δ3-10α-androsten
