16619-12-8

Basic information

• Product Name: 2-phenyl-2,3-dihydroinden-1-one
• Synonyms: 2-phenyl-2,3-dihydroinden-1-one;2-Phenyl-1-indanone;2,3-Dihydro-2-phenyl-1H-inden-1-one;2-Phenyl-2,3-dihydro-1H-inden-1-one
• CAS NO: 16619-12-8
• Molecular Formula: C₁₅H₁₂O
• Molecular Weight: 208.26
• Mol File: 16619-12-8.mol
• Article Data: 21

Chemical Properties

• Melting Point: 77.5°C
• Boiling Point: 335℃
• Flash Point: 144℃
• Appearance: /
• Density: 1.162
• Vapor Pressure: 0.000126mmHg at 25°C
• Refractive Index: 1.5361 (estimate)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-phenyl-2,3-dihydroinden-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-2,3-dihydroinden-1-one(16619-12-8)
• EPA Substance Registry System: 2-phenyl-2,3-dihydroinden-1-one(16619-12-8)

Safety Data

• Hazardous Substances Data: 16619-12-8(Hazardous Substances Data)

Usage

General Description

2-phenyl-2,3-dihydroinden-1-one is a chemical compound with a molecular formula C15H12O. It is a ketone with a phenyl group attached to the second carbon of a dihydroinden ring. 2-phenyl-2,3-dihydroinden-1-one is used in the synthesis of various organic compounds and pharmaceuticals due to its unique structure and reactivity. It has also been researched for potential biological activities, including antioxidant and anticancer properties. 2-phenyl-2,3-dihydroinden-1-one is a versatile compound with potential applications in the fields of chemistry and medicine.

InChI:InChI=1/C15H12O/c16-15-13-9-5-4-8-12(13)10-14(15)11-6-2-1-3-7-11/h1-9,14H,10H2

Upstream product

• 94942-89-9 2,3-diphenylpropanoic acid 
• 56042-76-3 2,3-diphenylpropionyl chloride 
• 19096-31-2 2-phenyl-1H-inden-1-one 
• 86738-88-7 2-phenyl-2-phenylthioindan-1-one 
• 201230-82-2 carbon monoxide 
• 501-65-5 diphenyl acetylene 
• 579-07-7 1-Phenylpropane-1,2-dione 
• 71-43-2 benzene 
• 103-82-2 phenylacetic acid 
• 100-44-7 benzyl chloride 
• 4452-11-3 1,2-diphenylprop-2-en-1-one 
• 7664-93-9 sulfuric acid 
• 621-82-9 Cinnamic acid 
• 108478-16-6 3-Hydroxy-1,2-diphenyl-1-propanone 

Downstream Products

• 2881-31-4 2-(2-oxo-2-phenylethyl)benzoic acid 
• 1961-97-3 3-phenyl-1H-indene 
• 4505-48-0 2-phenylindene 
• 5728-94-9 2-bromo-2-phenyl-indan-1-one 
• 131080-09-6 2-phenyl-1H-inden-3-yl acetate 
• 102018-40-6 (2-phenyl-inden-3-yl)-acetic acid ethyl ester 
• 18888-79-4 3-benzyl-2-phenyl-1H-indene 
• 102594-85-4 3-ethyl-2-phenyl-1H-indene 
• 10425-96-4 3-methyl-2-phenyl-1H-indene 
• 109037-03-8 2-Ethyl-2-phenyl-indanon-⁽¹⁾ 
• 1005420-27-8 (±)-2-methyl-2-phenyl-2,3-dihydro-1H-inden-1-one 
• 345298-67-1 2-Phenyl-1-o-tolyl-indan-1-ol 
• 61035-34-5 Bis(2-phenyl-3-indenyl) sulfide 
• 61035-31-2 2-phenyl-3-indenethiol 

Relevant articles and documents

Structures and reactivities of ethylene dication electrophiles

1,2-Dicarbonyl compounds such as 2,3-butanedione reacted with benzene in the presence of a strong acid, trifluoromethanesulfonic acid, to give gem-diphenylated ketones in high yield. The monoxime derivative of 1,2-diones also reacted with benzene in the a

Formal Enone α-Arylation via I(III)-Mediated Aryl Migration/Elimination

A formal enone α-arylation is described. This metal-free transformation relies on the I(III)-mediated skeletal reorganization of silyl enol ethers and features mild conditions, good yields, and high stereoselectivities for β-substituted enones.

B(C6F5)3-Catalyzed Highly Stereoselective Hydrogenation of Unfunctionalized Tetrasubstituted Olefins

A metal-free hydrogenation of unfunctionalized tetrasubstituted olefins were successfully realized using a combination of B(C6F5)3 and Ph2NMe catalyst. The corresponding products were afforded in 58-98% yields with up to >99:1 cis/trans selectivity.