59599-49-4

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate is also used as a building block for the synthesis of agrochemicals. Its properties allow it to be incorporated into the development of new pesticides, herbicides, and other agricultural chemicals to improve crop yields and protect against pests.
It is important to handle and use Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate with caution, as it may pose health and safety risks if not handled properly.

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 144464-63-1 5-oxo-5,6,7,8-tetrahydronaphthalen-1-yl trifluoromethanesulfonate 
• 930-68-7 cyclohexenone 
• 187808-48-6 methyl 5-(N,N-dimethylamino)-2,4-pentadienoate 
• 28315-93-7 5-Hydroxy-1-tetralone 

Relevant academic research and scientific papers

Tetralone derivatives as antiarrhythmic agents

Tetralone derivatives of the formula STR1 where R1 is halo, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, (aryl)alkenyl, (aryl)alkynyl, alkoxy, O-alkenyl, O-aryl, O-alkyl(heterocyclo), COO-alkyl,alkanoyl, CO-amino, CO-substituted amino, alkyl-CO-a

Aminodienylesters. I: The cycloaddition reactions of tert- aminodienylester with α,β-unsaturated carbonyl compounds, styrenes, and quinones

Methyl 5-(N,N-dimethylamino)-2,4-pentadienoate (tert-aminodienylester 1) was synthesized by condensation of methyl crotonate (2) with N,N,N',N'- tetramethylenediamine (3). The reactivity of 1 was investigated with methyl propiolate (4), dimethyl 2-butynedionate (5), dimethyl maleate (6), dimethyl fumarate (7), 2-buten-4-olide (8), 2-cyclohexenone (9), styrene (10), trans- β-nitrostyrene (11), 1,4-benzoquinone (19), methyl 1,4-naphthoquinone-5- carboxylate (21), 1,4-naphthoquinone (24), juglone (26), 5-methoxy-1,4- naphthoquinone (28), naphthazarin (31), and naphthazarin dimethyl ether (33). In addition, 5-(N,N-dimethylamino)-2,4-pentadienenitrile (tert-aminodienyl- nitrile 37) was synthesized by condensation of crotononitrile (36) with 3. The reactivity of 37 was investigated with dimethyl 2-butynedionate (5), and 2-cyclohexenone (9).

Synthesis of Benzoic and Tetralone Carboxylic Acid Esters from Phenols by Palladium Catalyzed Alkoxy/Aryloxy Carbonylation

Various phenols with an acyl group conjugated to the aromatic system were converted via trifluoromethanesulfonates into benzoic acid esters by a palladium catalyzed alkoxy/aryloxy carbonylation.