53575-46-5

Basic information

• Product Name: 1-methyl-1,3-diphenyl-1H-indene
• Synonyms: 1-methyl-1,3-diphenyl-1H-indene
• CAS NO: 53575-46-5
• Molecular Weight: 282.385
• Mol File: 53575-46-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-methyl-1,3-diphenyl-1H-indene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-1,3-diphenyl-1H-indene(53575-46-5)
• EPA Substance Registry System: 1-methyl-1,3-diphenyl-1H-indene(53575-46-5)

Safety Data

• Hazardous Substances Data: 53575-46-5(Hazardous Substances Data)

Upstream product

• 7664-93-9 sulfuric acid 
• 87734-88-1 1,1,3-triphenyl-buta-1,2-diene 
• 64-19-7 acetic acid 
• 1817-57-8 4-phenyl-3-butyne-2-one 
• 71-43-2 benzene 
• 857832-46-3 (+/-)-3-hydroxy-1.1.3-triphenyl-butene-⁽¹⁾ 
• 108-86-1 bromobenzene 
• 41231-78-1 (3E)-2,4-diphenylbut-3-en-2-ol 
• 800369-09-9 2-(4-methylphenyl)-4-phenylbut-3-yn-2-ol 
• 98-86-2 acetophenone 
• 5876-69-7 2,4-diphenylbut-3-yn-2-ol 
• 80221-02-9 4-(p-tolyl)but-3-yn-2-one 
• 536-74-3 phenylacetylene 
• 74-88-4 methyl iodide 

Downstream Products

• 96271-65-7 2-Benzoyl-1,3-diphenyl-1-methyl-inden 
• 1159-86-0 o-dibenzoylbenzene 
• 62747-73-3 3-methyl-1,2-diphenyl-1H-indene 
• 51310-25-9 1-methyl-2,3-diphenylindene 

Relevant articles and documents

Rhodium(III) porphyrin-catalyzed reactions via activation of alkynes

The cycloisomerization of 1,6-enynes catalyzed by rhodium(III) porphyr in under mild reaction conditions successfully afforded a five-membered ring system. The rhodium porphyrin was found to be a strong π-Lewis acid that could activate alkynes. Thus, rhod

Reactions of arylacetylenic compounds with arenes in the presence of aluminum halides

Conjugated arylacetylenic ketones and aldehydes, propargyl-type alcohols, and arylacetylenes reacted with arenes in the presence of AlBr3 or AlCl3 as catalyst to give substituted indenes. 3-Arylpropynoic acids under analogous conditi

Reaction of acetylene carbonyl compounds with benzene in the presence of aluminum bromide: A new preparation method for substituted indenes

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