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(6b)-6-Bromoandrost-4-ene-3,17-dione

Base Information
  • Chemical Name:(6b)-6-Bromoandrost-4-ene-3,17-dione
  • CAS No.:38632-00-7
  • Molecular Formula:C19H25BrO2
  • Molecular Weight:365.31
  • Hs Code.:
  • Mol file:38632-00-7.mol
(6b)-6-Bromoandrost-4-ene-3,17-dione

Synonyms:Androst-4-ene-3,17-dione,6b-bromo- (7CI);6b-Bromoandrost-4-ene-3,17-dione;6b-Bromoandrostenedione;

Suppliers and Price of (6b)-6-Bromoandrost-4-ene-3,17-dione
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 6β-BromoAndrostenedione
  • 10mg
  • $ 175.00
  • Chemenu
  • 6b-Bromoandrost-4-ene-3,17-dione 95%
  • 25g
  • $ 234.00
  • Chemenu
  • 6b-Bromoandrost-4-ene-3,17-dione 95%
  • 100g
  • $ 636.00
  • American Custom Chemicals Corporation
  • 6-BRONMANDROSTENEDIONE 95.00%
  • 5MG
  • $ 499.57
Total 103 raw suppliers
Chemical Property of (6b)-6-Bromoandrost-4-ene-3,17-dione
Chemical Property:
  • Vapor Pressure:6.77E-09mmHg at 25°C 
  • Melting Point:158-163°C (dec.) 
  • Refractive Index:1.577 
  • Boiling Point:467 °C at 760 mmHg 
  • Flash Point:100.3 °C 
  • PSA:34.14000 
  • Density:1.35 g/cm3 
  • LogP:4.46080 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:Chloroform (Slightly), Methanol (Very Slightly. Heated. Sonicated) 
Purity/Quality:

99% *data from raw suppliers

6β-BromoAndrostenedione *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • General Description (6b)-6-Bromoandrost-4-ene-3,17-dione is a brominated steroid derivative that serves as a key intermediate in the synthesis of modified androgens and potential aromatase inhibitors. It exists as a 6β-bromo epimer, which can undergo epimerization to the 6α-isomer under specific conditions, such as in carbon tetrachloride or chloroform-methanol mixtures. (6b)-6-Bromoandrost-4-ene-3,17-dione exhibits instability in methanol, leading to decomposition into 5α-androstane-3,6-dione derivatives. Additionally, it has been explored for its role in irreversible inactivation of human placental aromatase and as a substrate in Suzuki-Miyaura cross-coupling reactions to generate 6-arylated steroids, highlighting its utility in medicinal chemistry and steroid modification.
Technology Process of (6b)-6-Bromoandrost-4-ene-3,17-dione

There total 8 articles about (6b)-6-Bromoandrost-4-ene-3,17-dione 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:
Guidance literature:
With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; water; at 80 ℃; for 4h; Inert atmosphere;
DOI:10.1039/c2cc31973j
Guidance literature:
With N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane;
DOI:10.1016/0039-128X(79)90085-0
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