10271-32-6

Basic information

• Product Name: 1,1-dimethyl-3,3-diphenyl-2,3-dihydro-1H-indene
• Synonyms: 1,1-dimethyl-3,3-diphenyl-2,3-dihydro-1H-indene
• CAS NO: 10271-32-6
• Molecular Weight: 298.428
• Mol File: 10271-32-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,1-dimethyl-3,3-diphenyl-2,3-dihydro-1H-indene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dimethyl-3,3-diphenyl-2,3-dihydro-1H-indene(10271-32-6)
• EPA Substance Registry System: 1,1-dimethyl-3,3-diphenyl-2,3-dihydro-1H-indene(10271-32-6)

Safety Data

• Hazardous Substances Data: 10271-32-6(Hazardous Substances Data)

Upstream product

• 76-83-5 trityl chloride 
• 115-11-7 isobutene 
• 27144-18-9 3-(tritylthio) propanoic acid 
• 76-84-6 triphenylmethyl alcohol 
• 75-65-0 tert-butyl alcohol 
• 87549-81-3 tris[(triphenylstannyl)methyl]methane 
• 437-17-2 tritylium hexafluorophosphate 
• 50354-49-9 3,3,3-triphenylpropionic acid methyl ester 
• 4819-91-4 4,4,4-Triphenyl-2-methyl-butanol-(2) 

Downstream Products

• 10271-33-7 2-(2-benzoyl-phenyl)-2-methyl-propionic acid 

Relevant articles and documents

Direct Synthesis of Indanes via Iron-Catalyzed Dehydrative Coupling/Friedel–Crafts Cyclization of Two Different Alcohols

We report herein a novel iron-catalyzed cascade dehydrative coupling/Friedel–Crafts cyclization of two different alcohols, providing a variety of indanes, which are ubiquitous substructures found in natural products, pharmaceuticals, and functional materi

Scope and Limitations of Aliphatic Friedel-Crafts Alkylations. Lewis Acid Catalyzed Addition Reactions of Alkyl Chlorides to Carbon-Carbon Double Bonds

Lewis acid catalyzed addition reactions of alkyl halides 1 with unsaturated hydrocarbons 2 have been studied. 1:1 addition products 3 are formed if the addends 1 dissociate faster than the corresponding products 3; otherwise, polymerization of 2 takes place.For reaction conditions under which 1 and 3 exist mainly undissociated, solvolysis constants of model compounds can be used to predict the outcome of any such addition reactions if systems with considerable steric hindrance are excluded.