31981-44-9

Basic information

• Product Name: Gestonoronacetat
• Synonyms: 17-Acetyloxy-19-norpregn-4-ene-3,20-dione;17-Acetyloxy-19-norprogesterone;Gestonorone Acetat;19-Norpregn-4-ene-3,20-dione,17-(acetyloxy)-;GESTONORONE ACETATE;gestonoronacetat;19-NOR-3,20-DIOXOPREGNA-4-ENE-17-YL ACETATE;17-hydroxy-19-norpregn-4-ene-3,20-dione 17-acetate
• CAS NO: 31981-44-9
• Molecular Formula: C₂₂H₃₀O₄
• Molecular Weight: 358.47
• EINECS: 250-882-8
• Mol File: 31981-44-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 228-230°C
• Boiling Point: 490.2 °C at 760 mmHg
• Flash Point: 212.8 °C
• Appearance: /
• Density: 1.16
• Vapor Pressure: 9.35E-10mmHg at 25°C
• Refractive Index: 1.545
• Water Solubility: 3.62mg/L at 20℃
• CAS DataBase Reference: Gestonoronacetat(CAS DataBase Reference)
• NIST Chemistry Reference: Gestonoronacetat(31981-44-9)
• EPA Substance Registry System: Gestonoronacetat(31981-44-9)

Safety Data

• Hazardous Substances Data: 31981-44-9(Hazardous Substances Data)

Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C22H30O4/c1-13(23)22(26-14(2)24)11-9-20-19-6-4-15-12-16(25)5-7-17(15)18(19)8-10-21(20,22)3/h12,17-20H,4-11H2,1-3H3/t17-,18+,19+,20-,21-,22-/m0/s1

Upstream product

• 101766-63-6 3-hydroxy-19-norpregna-1,3,5⁽¹⁰⁾,16-tetraen-20-one 
• 95959-71-0 17α-Acetoxy-6β,19-epoxy-3,20-dioxo-Δ⁴-pregnen 
• 108-22-5 Isopropenyl acetate 
• 2137-18-0 17-alpha-Hydroxy-19-norprogesterone 
• 734-32-7 estra-4-ene-3,17-dione 
• 72-33-3 mestranol 
• 1624-62-0 estrone 3-methyl ether 
• 53-16-7 Estrone 
• 4824-92-4 19-Hydroxy-17α-acetoxy-3,20-dioxo-Δ⁴-pregnen 
• 14339-99-2 20,20-ethanediyldioxy-3-methoxy-19-nor-pregna-2,5⁽¹⁰⁾-dien-17-ol 
• 14328-46-2 20,20-(ethylenedioxy)-3-methoxy-17α-hydroxy-19-norpregna-1,3,5(10)-triene 
• 111979-17-0 16α,17-epoxy-3-methoxy-19-nor-pregna-1,3,5(10)-trien-20-one 
• 67519-64-6 16α,17α-epoxy-17-acetyl-Δ^1,3,5(10)-estratriene 
• 1624-58-4 17α-hydroxy-3-methoxy-19-norpregna-1,3,5(10)-trien-20-one 

Downstream Products

• 58652-19-0 17α-acetoxy-6-methylene-19-norpregn-4-ene-3,20-dione 
• 58652-20-3 nomegestrol acetate 

Relevant articles and documents

Nomegestrol intermediate synthesizing method

The invention provides a nomegestrol intermediate synthesizing method. The nomegestrol intermediate synthesizing method is characterized in that nomegestrol intermediate synthesis utilizes compound of 4-estrenochrysene-3,17-diketone as a beginning raw material; a nomegestrol intermediate crude product can be obtained through cyaniding, silyl etherification, intramolecular nucleophilic substitution reaction, reduction reaction and esterification reaction; then the nomegestrol intermediate can be obtained through methyl alcohol and ethyl acetate crystallization. The preparation method disclosed by the invention utilizes a short synthesizing line, the intermediate has stable performance, product yield is high, production cost is low, a production process is easy to control, environmental pollution is small, and industrial production is facilitated.