4834-33-7

Usage

Physical state

Colorless liquid

Odor

Sweet, floral

Uses

Intermediate in production of fragrances, dyes, and pharmaceuticals; solvent in industrial processes

Toxicity

Mildly toxic

Handling precautions

Handle with care

Environmental and health hazards

Potential hazards; proper safety measures required for handling and disposal

Upstream product

• 92104-77-3 2,4-dimethyl-4-phenyl-2-pentene 

Downstream Products

• 17610-14-9 1-(1,1,3,3-tetramethyl-2,3-dihydro-1H-inden-5-yl)ethan-1-one 
• 102168-26-3 Phenyl-(1,1,3,3-tetramethyl-indan-5-yl)-methanol 
• 17610-19-4 1-(6-isopropyl-1,1,3,3-tetramethyl-indan-5-yl)-ethanone 
• 71441-27-5 4'-[(E)-2-(1,1,3,3-tetramethyl-5-indanyl)propenyl]-acetophenone 
• 71441-25-3 p-[(E)-2-(1,1,3,3-tetramethyl-5-indanyl)vinyl]-benzoic acid ethyl ester 
• 71441-07-1 p-<(E)-2-(1,1,3,3-tetramethyl-5-indanyl)-propenyl>-benzoic acid ethylester 
• 69251-31-6 <1-(1,1,3,3-tetramethyl-5-indanyl)ethyl>-triphenylphosphonium bromide 
• 1394173-34-2 methyl 4-(1,1,3,3-tetramethylindan-5-ylethynyl)benzoate 

Relevant academic research and scientific papers

THE EFFECT OF THE POSITION OF THE DOUBLE BOND ON THE MECHANISM OF INTRAMOLECULAR CYCLOALKYLATION OF 2,4-DIMETHYL-4-PHENYLPENTENES IN SULFURIC ACID

Hydrogen exchange during the intramolecular cycloalkylation of 2,4-dimethyl-4-phenyylpentenes in 85percent sulfuric acid was studied by NMR and mass spectrometry. It was shown on the basis of the distribution of deuterium in 1,1,3,3-tetramethylindane that during cyclization of the endo-chain olefin the obtained γ-phenylalkyl cation undergoes partial deprotonation with the formation of an isomeric olefin whereas protonation of the terminal double bond is accompanied by rapid alkylation of the aromatic ring.