60235-06-5

Basic information

• Product Name: 6-(3,5-dimethoxyphenyl)hex-1-en-3-one
• Synonyms: 6-(3,5-dimethoxyphenyl)hex-1-en-3-one
• CAS NO: 60235-06-5
• Molecular Weight: 234.295
• Mol File: 60235-06-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-(3,5-dimethoxyphenyl)hex-1-en-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(3,5-dimethoxyphenyl)hex-1-en-3-one(60235-06-5)
• EPA Substance Registry System: 6-(3,5-dimethoxyphenyl)hex-1-en-3-one(60235-06-5)

Safety Data

• Hazardous Substances Data: 60235-06-5(Hazardous Substances Data)

Upstream product

• 80680-91-7 5-Bromo-2-methoxymethoxy-2-vinyl-pentanenitrile 
• 80680-93-9 5-(3,5-Dimethoxy-phenyl)-2-methoxymethoxy-2-vinyl-pentanenitrile 

Downstream Products

• 4244-18-2 2-[6-(3,5-dimethoxyphenyl)-3-oxohexyl]-2-ethylcyclopentane-1,3-dione 
• 80680-95-1 (R)-4-[2-(3,5-Dimethoxy-phenyl)-ethyl]-7a-methyl-2,3,7,7a-tetrahydro-6H-indene-1,5-dione 
• 80680-95-1 (S)-4-[2-(3,5-Dimethoxy-phenyl)-ethyl]-7a-methyl-2,3,7,7a-tetrahydro-6H-indene-1,5-dione 
• 80680-96-2 (1S,7aR)-4-[2-(3,5-Dimethoxy-phenyl)-ethyl]-1-hydroxy-7a-methyl-1,2,3,6,7,7a-hexahydro-inden-5-one 
• 80680-96-2 (1S,7aS)-4-[2-(3,5-Dimethoxy-phenyl)-ethyl]-1-hydroxy-7a-methyl-1,2,3,6,7,7a-hexahydro-inden-5-one 
• 80680-94-0 2-[6-(3,5-Dimethoxy-phenyl)-3-oxo-hexyl]-2-methyl-cyclopentane-1,3-dione 

Relevant articles and documents

A HIGHLY CONVERGENT AND FLEXIBLE STRATEGY FOR THE SYNTHESIS OF A-RING AROMATIC STEROIDS

Using Hendrickson's criteria for systematic synthesis design, a strategy featuring a linear six carbon synthon (7) for bis-annulation has been devised for economic, flexible and highly convergent syntheses of A-ring aromatic steroids.

Synthesis of 13-alkyl-gon-4-ones

The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.