2717-47-7

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

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

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 academic research and scientific papers

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.

Evolution of products in the combustion of scrap tires in a horizontal, laboratory scale reactor

A horizontal laboratory reactor was used to study the evolution of byproducts from the combustion of scrap tires at five nominal temperatures (ranging from 650 to 1050 °C) and different oxygen:sample ratios A model was used to calculate the bulk air ratio (λ), and the oxygen consumption was discussed considering this ratio λ. More than 100 volatile and semivolatile compounds were identified and quantified by gas chromatography mass spectrometry, plotting their yields vs the bulk air ratio and temperature. Five different behaviors considering the bulk air ratio and the temperature were identified.

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.