2613-76-5

Usage

Uses

Used in Food Industry:
1H-INDENE,2,3-DIHYDRO-1,1,3-T is used as a flavoring agent for its distinctive sweet, floral scent, enhancing the taste and aroma of various food products.
Used in Fragrance and Perfume Industry:
This chemical compound is utilized in the production of fragrances and perfumes, contributing to the creation of complex and appealing scents for a wide range of consumer products.
Used in Chemical Synthesis:
1H-INDENE,2,3-DIHYDRO-1,1,3-T serves as an intermediate in the synthesis of other chemicals, playing a crucial role in the development of new compounds and materials.
Used in Pharmaceutical Industry:
As an intermediate, 1H-INDENE,2,3-DIHYDRO-1,1,3-T is also involved in the synthesis of pharmaceuticals, aiding in the production of various medications and treatments.

InChI:InChI=1/C12H16/c1-9-8-12(2,3)11-7-5-4-6-10(9)11/h4-7,9H,8H2,1-3H3

Upstream product

• 107-41-5 2-methyl-2,4-pentanediol 
• 53875-83-5 4-chloro-4-methyl-1-pentetne 
• 71-43-2 benzene 
• 19219-84-2 (1,3-dimethylbutyl)benzene 
• 7446-70-0 aluminium trichloride 
• 98-82-8 Isopropylbenzene 
• 187737-37-7 propene 
• 120-12-7 anthracene 
• 188290-36-0 thiophene 
• 31516-55-9 2,4-diphenyl-2-methylpentane 
• 95-13-6 1-indene 

Relevant academic research and scientific papers

Acid-catalyzed Reactions of Aromatic Hydrocarbons with Alkanes and Cycloalkanes. X. Alkylations with Cyclohexane

The complex reaction mixtures of the nonconventional alkylation of benzene with cyclohexane in the presence of Lewis/proton acids and promotors were investigated by gas-liquid chromatography and mass spectrometry.Four representative groups of hydrocarbons were found including cycloalkylbenzenes, substituted indanes or tetralines (C12H16), C1-C6-alkylbenzenes and isomeric biscycloalkyls (C12H22).Their formation is interpreted as a competition between alkylation, (without or with isomerization), ringfission with cycloalkylation or fragmentation, and self-alkylation; phenylcycloalkylcations and phenylalkylcations are the intermediates.

Formylation and Acylation Reactions Catalysed by Trifluoromethanesulphonic Acid

Regioselective formylation of toluene, m- and p-xylene, and mesitylene has been achieved by carbonylation in trifluoromethanesulphonic acid at CO pressures of 90-125 atm.In the case of cumene, the formylation reaction is in competition with disproportionation to form di- and tri-isopropylbenzenes, leading to a complex product mixture.Slow addition of cyclohexene or cyclopentene to a mixture of benzene and CF3SO3H under a high CO pressure affords 4-cyclohexylbenzaldehyde and 4-cyclopentylbenzaldehyde in 34percent and 33percent yieds, respectively, while 2-methylbut-1-ene gives 2,2,3-trimethylindanone (39percent) under similar conditions.When cyclohexene is mixed with the acid under carbon monoxide (120 atm) before addition of benzene the major products are cyclohexyl phenyl ketone and cyclohexenyl cyclohexyl ketones.