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2324-11-0

(3,5,17)-17-Acetate Androstane-3,17-diol, also known as 17-acetoxy-5-androstan-3-ol, is a synthetic steroid compound derived from androstane. It is characterized by the presence of a 17-acetate group and a 3,17-diol structure, which gives it unique chemical properties. (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL is often used in scientific research and pharmaceutical applications, particularly in the development of anabolic steroids and other hormone-related medications. Its chemical formula is C21H32O3, and it has a molecular weight of 332.48 g/mol. The compound's structure and functional groups play a crucial role in its biological activity and potential therapeutic applications.

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  • 2324-11-0 Structure

  • Basic information

    1. Product Name: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL
    2. Synonyms: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL
    3. CAS NO:2324-11-0
    4. Molecular Formula: C21H34O3
    5. Molecular Weight: 334.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2324-11-0.mol

  • Chemical Properties

    1. Melting Point: 183-185 °C
    2. Boiling Point: 426.8±18.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.10±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 15.11±0.70(Predicted)
    10. CAS DataBase Reference: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL(2324-11-0)
    12. EPA Substance Registry System: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL(2324-11-0)

  • 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: 2324-11-0(Hazardous Substances Data)

2324-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2324-11-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2324-11:
(6*2)+(5*3)+(4*2)+(3*4)+(2*1)+(1*1)=50
50 % 10 = 0
So 2324-11-0 is a valid CAS Registry Number.

2324-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 17β-acetoxy-5α-androstan-3α-ol

1.2 Other means of identification

Product number -
Other names (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL

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:2324-11-0 SDS

2324-11-0Downstream Products

2324-11-0Relevant articles and documents

STEREOSELECTIVE REDUCTION OF C-2 SUBSTITUTED STEROID C-3 KETONES WITH LITHIUM TRIS-(R,S-1,2-DIMETHYLPROPYL)-BOROHYDRIDE AND SODIUM BOROHYDRIDE

Templeton, John F.,Kumar, V. P. Sashi,Gupta, R. K.,Friesen, Anne M.

, p. 339 - 346 (2007/10/02)

The effect of C-2 substitution on the stereoselective reduction of steroid C-3 ketones with lithium tris(R,S-1,2-dimethylpropyl)-borohydride and sodium borohydride was investigated.The C-2 mono- and di-substituted chloro and methyl derivatives were predominantly reduced to one of the epimeric alcohols.The 2α-chloro and 2α-methyl derivatives of 17β-acetoxy-5α-androstan-3-one undergo stereoselective reduction with lithium tris (R,S-1,2-dimethylpropyl)-borohydride to the axial (3α) alcohol as observed in the unsubstituted compound, whereas sodium borohydride gives predominantly the equatorial (3β) alcohol.The 2β-chloro, 2β-methyl, 2,2-dichloro, and 2,2-dimethyl derivatives are reduced predominantly to the equatorial (3β) alcohol by both reagents.

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