5037-63-8

Basic information

• Product Name: 5,8-DIMETHYL-1-TETRALONE
• Synonyms: 5,8-DIMETHYL-1-TETRALONE;AKOS BC-0948;5,8-Dimethyl-3,4-dihydro-1(2H)-naphthalenone;5,8-Dimethyltetralone;1,2,3,4-Tetrahydro-5,8-dimethylnaphthalene-1-one;3,4-Dihydro-5,8-dimethyl-1(2H)-naphthalenone;5,8-Dimethyltetralin-1-one;5,8-dimethyl-3,4-dihydro-2H-naphthalen-1-one
• CAS NO: 5037-63-8
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.24
• Mol File: 5037-63-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 33 °C
• Boiling Point: 313.5°Cat760mmHg
• Flash Point: 134.5°C
• Appearance: /
• Density: 1.054g/cm³
• Vapor Pressure: 0.000495mmHg at 25°C
• Refractive Index: 1.551
• CAS DataBase Reference: 5,8-DIMETHYL-1-TETRALONE(CAS DataBase Reference)
• NIST Chemistry Reference: 5,8-DIMETHYL-1-TETRALONE(5037-63-8)
• EPA Substance Registry System: 5,8-DIMETHYL-1-TETRALONE(5037-63-8)

Safety Data

• Hazardous Substances Data: 5037-63-8(Hazardous Substances Data)

Usage

General Description

5,8-Dimethyl-1-tetralone is a chemical compound with the molecular formula C12H16O. It is a ketone and a member of the tetralone family, which is characterized by a bicyclic structure with a ketone functional group. 5,8-DIMETHYL-1-TETRALONE is a colorless liquid at room temperature and is primarily used as an intermediate in the synthesis of other organic compounds. It is commonly used in the pharmaceutical and chemical industries for the production of various drugs and fine chemicals. 5,8-Dimethyl-1-tetralone also has potential applications in organic synthesis and medicinal chemistry due to its unique structural features and reactivity. Additionally, it may have biological activity and is a subject of research for its potential pharmacological properties.

InChI:InChI=1/C12H14O/c1-8-6-7-9(2)12-10(8)4-3-5-11(12)13/h6-7H,3-5H2,1-2H3

Upstream product

• 96-48-0 4-butanolide 
• 106-42-3 para-xylene 
• 4635-59-0 4-Chlorobutanoyl chloride 
• 71526-84-6 2',5'-dimethyl-4-chlorobutyrophenone 
• 930-68-7 cyclohexenone 
• 74-99-7 prop-1-yne 

Downstream Products

• 30098-36-3 1,2,3,4-Tetrahydro-5,8-dimethyl-7-bromnaphthalin-1-on 
• 85973-17-7 5,6,8,9-tetrahydro-1,4-dimethyl-7-phenyldibenzacridine 
• 85973-16-6 5,6-dihydro-7,10-dimethyl-2,4-diphenylbenzoquinoline 
• 85973-20-2 5,6-dihydro-7,10-dimethyl-4-phenyl-2-t-butylbenzoquinoline 
• 56162-01-7 5,8-Dimethyl-4-p-tolyl-1,2-dihydro-naphthalene 
• 56162-00-6 5,8-Dimethyl-4-phenyl-1,2-dihydro-naphthalene 
• 13621-25-5 5,7-dimethyltetralone 
• 1453-06-1 4-(p-xylyl)butyric acid 
• 23702-41-2 1-Oxo-5,8-dimethyl-2-(2-isobutyrylcyclohexyl)-tetralin 
• 85973-04-2 5,6-dihydro-7,10-dimethyl-2,4-diphenylbenzochromenylium trifluoromethanesulphonate 
• 80710-75-4 5,8-Dimethyl-1-p-tolyl-1,2,3,4-tetrahydro-naphthalen-1-ol 
• 85990-49-4 5,6,8,9-tetrahydro-1,4-dimethyl-7-phenyldibenzoxanthylium trifluoromethanesulphonate 
• 109381-28-4 5,8-dimethyl-2-(phenylmethyl)-1-naphthol 
• 32820-12-5 5,8-Dimethyl-1-tetralol 

Relevant articles and documents

PROCESS FOR PRODUCING AROMATIC COMPOUNDS BY FRIEDEL-CRAFTS REACTION

There is provided a process for producing an aromatic compound by Friedel-Crafts reaction product, which comprises reacting an aromatic compound with an ester compound in the presence of a heteropolyacid-containing solid acid catalyst.

A new synthesis of occidol

Sodium borohydride reduction of 5,8-dimethyl-3,4-dihydronaphthalen-1-(2H)-one (4) yielded 5,8-dimethyl-1,2,3,4-tetrahydro-1-naphthol (5). The tetralol 5 on Vilsmeier-Haack reaction with N,N-dimethylacetamide yielded 1-(5,8-dimethyl-3,4-dihydro-2-naphthyl)

Synthesis of 1,4-, 2,4-, and 3,4-dimethylphenanthrenes: A novel deoxygenation of arene 1,4-endoxides with trimethylsilyl iodide

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