2717-47-7

Basic information

• Product Name: 1,2-Dihydro-6-methylnaphthalene
• Synonyms: 1,2-Dihydro-6-methylnaphthalene
• CAS NO: 2717-47-7
• Molecular Formula: C₁₁H₁₂
• Molecular Weight: 144.21
• Mol File: 2717-47-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 223.4°C at 760 mmHg
• Flash Point: 82.5°C
• Appearance: /
• Density: 0.988g/cm³
• Vapor Pressure: 0.144mmHg at 25°C
• Refractive Index: 1.564
• CAS DataBase Reference: 1,2-Dihydro-6-methylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Dihydro-6-methylnaphthalene(2717-47-7)
• EPA Substance Registry System: 1,2-Dihydro-6-methylnaphthalene(2717-47-7)

Safety Data

• Hazardous Substances Data: 2717-47-7(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Odor

Sweet, aromatic

Uses

Production of fragrances
Solvent
Intermediate in the synthesis of various organic compounds
Raw material in the manufacturing of dyes, resins, and other chemicals

Hazardous substance

Yes

Safety precautions

Proper handling and storage required

Handling and disposal procedures

Follow proper guidelines to prevent harm to human health and the environment

InChI:InChI=1/C11H12/c1-9-6-7-10-4-2-3-5-11(10)8-9/h3,5-8H,2,4H2,1H3

Upstream product

• 6938-36-9 7-Methyl-1,2,3,4-tetrahydro-[1]naphthol 
• 32281-97-3 7-bromo-3,4-dihydro-2H-naphthalen-1-one 
• 75693-15-1 7-bromo-1,2,3,4-tetrahydronaphthalen-1-ol 
• 4521-22-6 4-(4-methylphenyl)butyric acid 
• 22009-37-6 7-methyl-3,4-dihydro-2H-naphthalen-1-one 
• 75693-17-3 bromo-7 dihydro-3,4 naphthalene 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 1680-51-9 6-methyl-1,2,3,4-tetrahydronaphthalene 
• 51015-29-3 6-methyl-3,4-dihydronaphthalen-1(2H)-one 
• 91-57-6 2-Methylnaphthalene 

Relevant articles and documents

Catalytic asymmetric intermolecular bromoesterification of unfunctionalized olefins

An asymmetric intermolecular bromoesterification of unfunctionalized olefins catalyzed by (DHQD)2PHAL is described. Optically active bromoesters can be obtained with up to 92% ee.

Synthesis of Biological Markers in Fossil Fuels. 2. Synthesis and 13C NMR Studies of Substituted Indans and Tetralins

Unambiguous syntheses of all possible methyl, ethyl, n-propyl, and n-butyl derivatives of indan and tetralin were developed using the Kumada coupling procedure involving the reaction of aryl or vinyl halides with Grignard reagents in the presence of nickel(II) chloride.An analysis of the 13C NMR spectra of these compounds was also completed.