13225-63-3

Basic information

• Product Name: 2,3-Dihydro-4-phenyl-1H-benzindene
• Synonyms: 2,3-Dihydro-4-phenyl-1H-benzindene
• CAS NO: 13225-63-3
• Molecular Weight: 244.336
• Mol File: 13225-63-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,3-Dihydro-4-phenyl-1H-benzindene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dihydro-4-phenyl-1H-benzindene(13225-63-3)
• EPA Substance Registry System: 2,3-Dihydro-4-phenyl-1H-benzindene(13225-63-3)

Safety Data

• Hazardous Substances Data: 13225-63-3(Hazardous Substances Data)

Upstream product

• 49769-17-7 1,7-diphenylhepta-1,6-diyne 
• 172607-53-3 phenyl 2-(trimethylsilylethynyl)phenyl ketone 
• 936-52-7 1-(N-morpholino)cyclopent-1-ene 
• 308378-45-2 (2-ethynylphenyl)(phenyl)methanone 
• 1614-92-2 1-(N-piperidino)cyclopentene 
• 7188-22-9 1-phenylphthalazine 

Relevant articles and documents

Thermal and Au(I)-catalyzed intramolecular [4+2] cycloaddition of aryl-substituted 1,6-diynes for the synthesis of biaryl compounds

1,6-Diynes, possessing aryl groups on their termini, undergo an intramolecular [4+2] cycloaddition via strained cyclic allene intermediates to give various biaryl compounds. Under thermal conditions, isomerization of the intermediates occurs, while, in th

Gold-catalyzed synthesis of bicyclo[4.3.0]nonadiene derivatives via tandem 6-endo-dig/Nazarov cyclization of 1,6-allenynes

(Chemical Equation Presented) Catalytic cyclization of 1,6-allenynes was achieved by AuPPh3SbF6 (5 mol %) in cold CH 2Cl2 (0°C, 0.5-4 h) to form bicyclo[4.3.0]nonadiene products; this cyclization proceeded more

Novel synthesis of pentacarbonylbenzopyranylidenetungsten(0) complexes and their Diels - Alder reaction with electron-rich alkenes [11]

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