3344-45-4

Usage

Chemical compound

3-Methyl-1,2,3,4-tetrahydronaphthalene-1-ol

Also known as

3-Methyl-1-tetralol

Properties

Colorless liquid
Sweet, floral odor
Found in essential oils such as rose and jasmine

Uses

Production of fragrances and flavorings
Manufacturing of perfumes and scented products
Flavoring agent in the food and beverage industry

Importance

Enhances and extends fragrance of other ingredients
Adds sweet and floral taste to various products
Plays a key role in creating appealing scents and flavors for consumer goods

Upstream product

• 14944-23-1 3-methyl-1-tetralone 
• 58-27-5 menadione 
• 6630-33-7 ortho-bromobenzaldehyde 
• 111539-90-3 N,N-Diethyl-2-[hydroxy-((6R,8R)-8-hydroxy-6-methyl-5,6,7,8-tetrahydro-naphthalen-1-yl)-methyl]-6-methoxy-benzamide 
• 22436-06-2 2-methyl-3-phenylpropanol 
• 111539-93-6 3-methyl-8-formyl-cis-1-tetralol 
• 83303-64-4 3-Methyl-4-phenylbutanenitrile 
• 111539-83-4 Toluene-4-sulfonic acid 2-methyl-3-phenyl-propyl ester 
• 111539-81-2 ethyl 3-methyl-4-(1,3-dithiopropano)-4-phenylbutyrate 
• 72277-22-6 3-Methyl-4-phenyl-butansaeure-ethylester 
• 5425-44-5 2-Phenyl-[1,3]dithiane 
• 111539-92-5 (6R,8R)-8-Methoxymethoxy-6-methyl-5,6,7,8-tetrahydro-naphthalene-1-carbaldehyde 
• 34599-62-7 ethyl 2-ethoxycarbonyl-3-methyl-4-phenylbutanoate 

Downstream Products

• 111539-90-3 N,N-Diethyl-2-[hydroxy-((6R,8R)-8-hydroxy-6-methyl-5,6,7,8-tetrahydro-naphthalen-1-yl)-methyl]-6-methoxy-benzamide 
• 111539-96-9 2-Methoxy-6-(6-methyl-8-oxo-5,6,7,8-tetrahydro-naphthalen-1-ylmethyl)-benzoic acid 
• 96239-80-4 2-Methoxy-6-(6-methyl-5,6-dihydro-naphthalen-1-ylmethyl)-benzoic acid 

Relevant academic research and scientific papers

Regioselective synthesis of substituted 1-indanols, 2,3-dihydrobenzofurans and 2,3-dihydroindoles by electrochemical radical cyclization using an arene mediator

Electrochemical reduction of haloarenes carrying 2-(1-hydroxybut-3-enyl), 2-allyloxy or N-allyl-N-methylamino group in the presence of phenanthrene as a mediator generated the corresponding aryl radicals and gave the corresponding 5-exo cyclization produc

Regioselective Radical Cyclization by Electrochemical Reduction Using an Arene Mediator. Environmentally Benign Method

Electrochemical reduction of 2-(but-3-enyl)-1-haloarenes in the presence of phenanthrene as a mediator generated the corresponding aryl radicals and gave cyclized products in good yields. Higher regio- and stereoselectivities than those of usual radical cyclization using AIBN-TBTH were achieved.

Directed ortho metalation reactions. Convergent synthesis of "angular" anthracyclinones ochromycinone and X-14881 C

Convergent syntheses of the benzanthraquinone natural products X-14881 C (2c) and ochromycinone (2d) have been achieved using aromatic directed metalation strategies.Key steps involve (a) the condensations of dilithiated cis-tetralol (13a) with the ald

DIRECTED ORTHO METALATION REACTIONS. SYNTHESIS OF NATURALLY-OCCURRING BENZANTHRAQUINONES X-14881 C AND OCHROMYCINONE

The synthesis of the benzanthraquinone natural products X-14881 C (1c) and ochromycinone (1a) via an aromatic directed metalation strategy (Scheme 1) is described.

SYNTHESE DU METHOXYCARBONYL-3 INDENE ET DE METHOXYCARBONYL-4 DIHYDRO-1,2 NAPHTALENES. OBTENTION DES β-TETRALONES A PARTIR DES α-TETRALONES CORRESPONDANTES

The synthesis of variously substituted 3-methoxycarbonylindene and 4-methoxycarbonyl-1,2-dihydronaphthalenes is described.A simple and efficient method for the transformation of 1-tetralone into 2-tetralone is reported.