1232-88-8

Basic information

• Product Name: 8-methoxy-12a-methyl-3,4,4a,4b,5,6,10b,11,12,12a-decahydrochrysen-2(1H)-one
• CAS NO: 1232-88-8
• Molecular Formula: C₂₀H₂₆O₂
• Molecular Weight: 298.4192
• Mol File: 1232-88-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 441.5°C at 760 mmHg
• Flash Point: 186.5°C
• Density: 1.083g/cm³
• Vapor Pressure: 5.43E-08mmHg at 25°C
• Refractive Index: 1.547
• CAS DataBase Reference: 8-methoxy-12a-methyl-3,4,4a,4b,5,6,10b,11,12,12a-decahydrochrysen-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 8-methoxy-12a-methyl-3,4,4a,4b,5,6,10b,11,12,12a-decahydrochrysen-2(1H)-one(1232-88-8)
• EPA Substance Registry System: 8-methoxy-12a-methyl-3,4,4a,4b,5,6,10b,11,12,12a-decahydrochrysen-2(1H)-one(1232-88-8)

Safety Data

• Hazardous Substances Data: 1232-88-8(Hazardous Substances Data)

Upstream product

• 2930-75-8 3-Methoxy-D-homo-8α-oestra-1,3,5(10)-trien-17aβ-ol 
• 878-47-7 (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one 
• 65083-12-7 17aβ-(t-Butoxy)-3-methoxy-D-homo-9,10-secooestra-1,3,5(10),8(14)-tetraen-6,9-dion 
• 61950-53-6 1β-tert-butoxy-8aβ-methyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-6-one 
• 2000-72-8 3-methoxy-D-homoestra-1,3,5⁽¹⁰⁾,8-tetraen-17a-one 
• 1193-55-1 2-methylcyclohexane-1,3-dione 
• 1456-49-1 DL-3-methoxy-D-homoestra-1,3,5⁽¹⁰⁾,8,14-pentaen-17a-one 
• 5067-45-8 2-<2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ylidene)ethyl>-2-methylcyclohexane-1,3-dione 
• 2146-61-4 3-methoxyphenethyl bromide 
• 21506-72-9 10-Methyl-1-(3-methoxy-phenethyl)-2,5-dioxo-Δ¹⁽⁹⁾-octalin 
• 20007-99-2 Wieland-Miescher ketone 
• 1094-04-8 3-Methoxy-D-homo-oestratetraen-(1,3,5⁽¹⁰⁾,9⁽¹¹⁾)-on-(17a) 
• 972-24-7 9β-methyl-5-(3-methoxy-phenethyl)-trans-decalindion-(1,6) 
• 7082-74-8 8-hydroxy-12a-methyl-3,5,6,11,12,12a-hexahydro-2H-chrysen-1-one 

Downstream Products

• 2000-70-6 D-Homo-8-isoestrone 

Relevant articles and documents

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A new strategy for the construction of A-ring aromatic steroids which resulted in the formal total synthesis of estrone is described.Thus reaction of the adduct (9), obtained from 1-methoxy-4-methylcyclohexa-1,4-diene and acrolein, with 3-(m-methoxyphenyl

BIOLOGICAL ACTIVITY OF RACEMIC D-HOMO-8-ISOESTRONE

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