58526-32-2

Basic information

• Product Name: 2-[3-(acetyloxy)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name)
• CAS NO: 58526-32-2
• Molecular Formula: C₂₄H₃₈O₄
• Molecular Weight: 390.5561
• Mol File: 58526-32-2.mol

Chemical Properties

• Boiling Point: 497°C at 760 mmHg
• Flash Point: 161.4°C
• Density: 1.11g/cm³
• Vapor Pressure: 3.13E-11mmHg at 25°C
• Refractive Index: 1.532
• CAS DataBase Reference: 2-[3-(acetyloxy)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[3-(acetyloxy)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name)(58526-32-2)
• EPA Substance Registry System: 2-[3-(acetyloxy)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoic acid (non-preferred name)(58526-32-2)

Safety Data

• Hazardous Substances Data: 58526-32-2(Hazardous Substances Data)

Usage

Class

Nonsteroidal anti-inflammatory drug (NSAID)

Function

Reduces pain, fever, and inflammation by inhibiting the production of certain chemicals in the body that cause inflammation

Additional use

Prevents and treats heart attacks, strokes, and blood clots by preventing the formation of blood clots

Commonly sold over the counter

Under various brand names

Caution advised

Should be used under the guidance of a healthcare professional due to potential side effects and interactions with other medications.

Upstream product

• 4057-86-7 3α-acetoxy-24-nor-5α-cholanoic acid-(23)-methyl ester 
• 15238-53-6 3α-hydroxy-24-nor-5α-cholanoic acid-(23)-methyl ester 
• 4057-88-9 3α-acetoxy-24-nor-5α-cholanoic acid-(23) 
• 65444-87-3 3β-tert-butyldimethylsilyloxy-5α,17β-pregnan-20-one 
• 4651-48-3 acetic acid stigmasteryl ester 
• 32212-73-0 5α,6β-dibromostigmastan-3β-yl acetate 
• 67-66-3 chloroform 
• 64-19-7 acetic acid 
• 56-23-5 tetrachloromethane 
• 128-08-5 N-Bromosuccinimide 
• 4144-29-0 acetic acid-(24.24-diphenyl-5α-cholen-(23)-yl-(3β)-ester) 
• 60-29-7 diethyl ether 
• 1474-14-2 3β-acetoxybisnor-5-cholenic acid 
• 15467-89-7 (20S)-23,24-Bisnor-5α-cholan-3β-ol-22-carboxaldehyd-acetat 

Downstream Products

• 474-51-1 20α-dimethylamino-5α-pregnan-3β-ol 

Relevant articles and documents

Ionic hydrogenation-directed stereoselective construction of C-20(H) stereogenic center in steroid side chains: Scope and limitations

Stereoselective synthesis of steroidal C-20 tertiary alcohols with n-butyl, vinyl, furyl, thienyl, thiazolyl, aryl and pyridyl side chains via Grignard reaction or organolithium reagents have been realized starting from readily available 16-dehydropregnen

Modified Pyridinium Chlorochromate Oxidation of Aldehydes to Carbamoyl Azides/Acyl Azides or Carboxylic Acids

Aldehydes are transformed into carbamoyl azides/acyl azides by pyridinium chlorochromate in the presence of sodium azide.Comparable oxidations modified with sodium cyanide generate carboxylic acids from simple aliphatic aldehydes whereas conjugated aldehydes are undeactive.