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24516-38-9

(6beta)-6-bromopregn-4-ene-3,20-dione is a synthetic steroid hormone belonging to the pregnane steroid class. It features a bromine atom at the 6th position and ketone groups at the 3rd and 20th positions of the steroid structure. (6beta)-6-bromopregn-4-ene-3,20-dione has the potential to exhibit hormonal activity in biological systems due to its ability to interact with steroid receptors and modulate hormonal signaling pathways. The presence of the bromine atom in the molecule may also provide specific chemical properties that could be beneficial for certain applications, suggesting potential biological and pharmaceutical relevance.

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  • 24516-38-9 Structure

  • Basic information

    1. Product Name: (6beta)-6-bromopregn-4-ene-3,20-dione
    2. Synonyms: (6beta)-6-Bromopregn-4-ene-3,20-dione; 6beta-Bromoprogesterone; Pregn-4-ene-3,20-dione, 6-bromo-, (6beta)-
    3. CAS NO:24516-38-9
    4. Molecular Formula: C21H29BrO2
    5. Molecular Weight: 393.3578
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24516-38-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 481.1°C at 760 mmHg
    3. Flash Point: 83°C
    4. Appearance: N/A
    5. Density: 1.29g/cm3
    6. Vapor Pressure: 2.05E-09mmHg at 25°C
    7. Refractive Index: 1.565
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (6beta)-6-bromopregn-4-ene-3,20-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: (6beta)-6-bromopregn-4-ene-3,20-dione(24516-38-9)
    12. EPA Substance Registry System: (6beta)-6-bromopregn-4-ene-3,20-dione(24516-38-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 24516-38-9(Hazardous Substances Data)

24516-38-9 Usage

Uses

Used in Pharmaceutical Research and Development:
(6beta)-6-bromopregn-4-ene-3,20-dione is used as a research compound for its potential hormonal activity. It is particularly valuable in the study of steroid receptors and hormonal signaling pathways, which are crucial for understanding various physiological processes and developing targeted therapies for related conditions.
Used in Drug Design and Synthesis:
The unique chemical structure of (6beta)-6-bromopregn-4-ene-3,20-dione, including the bromine atom, makes it a useful building block or starting material for the design and synthesis of new steroidal drugs. Its specific chemical properties can be exploited to create novel compounds with improved pharmacological profiles or targeted applications.
Used in Hormonal Regulation Studies:
(6beta)-6-bromopregn-4-ene-3,20-dione is used as a model compound in the investigation of hormonal regulation mechanisms. Understanding how this compound interacts with steroid receptors can provide insights into the development of new treatments for hormonal imbalances and related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 24516-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24516-38:
(7*2)+(6*4)+(5*5)+(4*1)+(3*6)+(2*3)+(1*8)=99
99 % 10 = 9
So 24516-38-9 is a valid CAS Registry Number.

24516-38-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6β-bromo-4-pregnene-3,20-dione

1.2 Other means of identification

Product number -
Other names 6β-bromoprogesterone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24516-38-9 SDS

24516-38-9Relevant articles and documents

Synthesis of 11α-hydroxyprogesterone haptens

Yoshida, Hirokazu,Nakai, Shiro,Nimbari, Fusako,Yoshimoto, Kiyoko,Nishimura, Tadashi

, p. 727 - 738 (2007/10/02)

C-4 and C-6 bridged haptens of 11α-hydroxyprogesterone, an anti-androgen, were respectively synthesized via 4,5 and 5α,6α epoxide ring openings using 3-mercaptopropanoic acid.Substitution of 6-bromo derivative of progesterone using the same reagent unexpectedly afforded a C-4 substituted product instead of the normal C-6 substituted product previously reported in the literature.

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