1444-59-3

Usage

Uses

Used in Food and Beverage Industry:
1-Hexen-3-one, 6-(3-methoxyphenyl)is used as a flavoring agent in the food and beverage industry for its fruity and floral aroma, enhancing the taste and smell of various products.
Used in Perfumery:
In the perfume industry, 1-Hexen-3-one, 6-(3-methoxyphenyl)is utilized as a fragrance ingredient, contributing to the creation of complex and pleasant scents in perfumes and other scented products.
Used in Chemical Production:
1-Hexen-3-one, 6-(3-methoxyphenyl)is also used in the manufacture of other chemicals, serving as a building block or intermediate in the synthesis of various compounds.
Used in Pharmaceutical Research:
1-Hexen-3-one, 6-(3-methoxyphenyl)has been studied for its potential therapeutic properties, including antimicrobial and anti-inflammatory effects, indicating its possible use in the development of new drugs and treatments.
Used in Cosmetics Industry:
Given its pleasant aroma and potential therapeutic properties, 1-Hexen-3-one, 6-(3-methoxyphenyl)may also find applications in the cosmetics industry, where it could be used in the formulation of fragrances and other scented products with added benefits.

Upstream product

• 408523-53-5 6-(3-methoxyphenyl)hex-1-en-3-ol 
• 80680-92-8 2-Methoxymethoxy-5-(3-methoxy-phenyl)-2-vinyl-pentanenitrile 
• 60235-09-8 1-bromo-6-(m-methoxyphenyl)hexan-3-one 
• 70-29-1 diethyl sulphide 
• 57816-04-3 methyl 4-(3-methoxyphenyl)butanoate 
• 57816-06-5 2-Benzenesulfinyl-6-(3-methoxy-phenyl)-hexan-3-one 
• 1424-71-1 1-diethylamino-6-(m-methoxyphenyl)-2-hexyne 
• 57816-02-1 5-(3-methoxyphenyl)-1-methylsulfinyl-pentan-2-one 
• 74-88-4 methyl iodide 
• 1826-67-1 vinyl magnesium bromide 
• 281224-85-9 4-(5-methoxy-2-methyl-phenyl)-butyraldehyde 
• 19614-12-1 2-bromo-5-methoxybenzyl bromide 
• 149244-21-3 1-bromo-2-(but-3-en-1-yl)-4-methoxybenzene 
• 328570-79-2 4-methyl-3-(4-hydroxybutyl)anisole 

Downstream Products

• 1823-11-6 6-m-Methoxyphenylhexan-3-on 
• 2627-90-9 13β-propyl-3-methoxygona-1,3,5(10),8-tetraen-17-one 
• 18300-15-7 3-methoxy-9,10-secoestra-1,3,5⁽¹⁰⁾,8⁽¹⁴⁾-tetraene-9,17-dione 
• 178275-48-4 (2R,3S,4R,5R)-2-(6-m-methoxyphenyl-3-oxohexyl)-3-hydroxy-2,4,5-trimethylcyclopentanone 
• 178275-49-5 (1S,3R,6R,8S,9S)-1-hydroxy-3-(3-m-methoxyphenylpropyl)-6,8,9-trimethyl-2-oxabicyclo[4.3.0]nonan-7-one 
• 40445-85-0 2-(6'-m-Methoxyphenyl-3'-oxohexyl)-2,3-dimethoxycarbonyl-4-methylcyclopentanon 
• 134329-65-0 1-(1-methoxy-4-methylbicyclo<2.2.2>oct-5-en-2-yl)-4-(3-methoxyphenyl)butan-1-one 
• 60235-19-0 2-(6-m-methoxyphenyl-3-oxohexyl)-2-propylcyclohexane-1,3-dione 

Relevant academic research and scientific papers

Synthesis of (-)-astrogorgiadiol

Reaction of Rh2(S)-PTPA4 with the (R)-citronellol-derived α-diazo-β-ketoester 1 led to the formation of cyclic β-ketoester 2 in 95% yield and 48% diastereomeric excess. The purity of 2 was increased to >99% de after one crystallization. To demonstrate its utility in steroid total synthesis, the β-ketoester 2 was carried on to secosteroid (-)-astrogorgiadiol (3), a naturally occuring vitamin D analogue with antiproliferative properties.

Synthesis Based on Cyclohexadienes. V. A New Approach to the Synthesis of A-Ring Aromatic Steroids: a Formal Total Synthesis of (+/-)-Estrone

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

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.

TOTAL SYNTHESIS OF STEROIDS. PART XV. A NOVEL METHOD OF SYNTHESIS OF β-AMINO KETONES AND VINYL KETONES AND ITS APPLICATION IN TOTAL SYNTHESIS OF ESTROGENS

A new method of synthesizing β-bromo ketones, vinyl ketones and β-N,N-dimethylamino ketones, starting from terminal olefines, diborane and 1-diazo-4-bromo-2-butanone has been described.The above method was utilized in total synthesis of estrogens.

Synthesis of gon-4-enes

1. A therapeutic composition having progestational activity comprising as active ingredient a 17-aliphatic carboxylic acid ester of 17α-ethynyl-18-methyl-19-nortestosterone and a pharmaceutical carrier for said compound.

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.