6339-17-9

Basic information

• Product Name: (3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol
• Synonyms: (3beta,5alpha,11beta,17beta)-9-Fluoro-17-methylandrostane-3,11,17-triol; 9.alpha.-Fluoro-17.alpha.-methyl-5.alpha.-Androstan-3.beta.,11.beta.,17.beta.-triol; 9-Fluoro-17alpha-methyl-5alpha-androstane-3beta,11beta,17-triol
• CAS NO: 6339-17-9
• Molecular Formula: C₂₀H₃₃FO₃
• Molecular Weight: 340.4726
• Mol File: 6339-17-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 458.2°C at 760 mmHg
• Flash Point: 230.9°C
• Density: 1.19g/cm³
• Vapor Pressure: 2.55E-10mmHg at 25°C
• Refractive Index: 1.554
• CAS DataBase Reference: (3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol(6339-17-9)
• EPA Substance Registry System: (3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol(6339-17-9)

Safety Data

• Hazardous Substances Data: 6339-17-9(Hazardous Substances Data)

Usage

Description

(3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol is a synthetic steroid compound with a fluorine atom and a methyl group at specific positions on the steroid backbone. It has a triol structure, meaning it contains three hydroxyl groups on the steroid ring. (3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol may have potential pharmaceutical or research applications, as modifications to the steroid backbone can alter its biological activity. The specific positioning and combination of functional groups in this compound may confer unique properties that could be of interest for further study in the fields of pharmacology, endocrinology, and biochemistry.

Uses

Used in Pharmaceutical Industry:
(3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol is used as a pharmaceutical compound for its potential therapeutic effects. The unique structure and functional groups of this compound may provide novel mechanisms of action and therapeutic benefits in the treatment of various diseases and conditions.
Used in Research Applications:
(3beta,5alpha,11beta,17beta)-9-fluoro-17-methylandrostane-3,11,17-triol is used as a research compound for studying the structure-activity relationships of steroidal compounds. The specific positioning of the fluorine and methyl groups, along with the triol structure, may provide insights into the biological activity and potential applications of this compound in various research areas, such as endocrinology and biochemistry.

Upstream product

• 51773-60-5 11β,17β-Dihydroxy-17α-methyl-9α-fluoro-5α-androstan-3-one