13578-98-8

Basic information

• Product Name: 2,2-dibenzyl-1-indanone
• Synonyms: 2,2-dibenzyl-1-indanone
• CAS NO: 13578-98-8
• Molecular Formula: C₂₃H₂₀O
• Molecular Weight: 312.4043
• Mol File: 13578-98-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-dibenzyl-1-indanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dibenzyl-1-indanone(13578-98-8)
• EPA Substance Registry System: 2,2-dibenzyl-1-indanone(13578-98-8)

Safety Data

• Hazardous Substances Data: 13578-98-8(Hazardous Substances Data)

Upstream product

• 91158-87-1 2,2-dibenzyl-2,3-dihydro-1H-indene-1,3-dione 
• 16307-30-5 2-benzyl-1-indanone 
• 100-44-7 benzyl chloride 
• 83-33-0 inden-1-one 
• 606-23-5 1H-indene-1,3(2H)-dione 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Silylative Kinetic Resolution of Racemic 2,2-Dialkyl 5- and 6-Membered Cyclic Benzylic Alcohol Derivatives Catalyzed by Chiral Guanidine, (R)-N-Methylbenzoguanidine

Efficient silylative kinetic resolution of racemic 2,2-dialkyl 5- and 6-membered cyclic benzylic alcohols was achieved using diphenylmethylchlorosilane (Ph2MeSiCl) or phenyldimethylchlorosilane (PhMe2SiCl) as a silyl source catalyzed by chiral guanidine. The reaction could be applied to a broad range of 2,2-dialkyl 1-indanols with good s-values, irrespective of the electronic nature of the substituent on the aromatic ring of the substrates and the type of substituent at the C2-position. In addition, several 2,2-dimethyl 6-membered cyclic and heterocyclic alcohols could be adopted in the reaction. (Figure presented.).

Benzoanellated Centropolyquinanes, 15. - Benzoanellated Fenestranes with , , and Frameworkes: The Route from 1,3-Indandione to Fenestrindan

The synthesis and spectroscopic characterization of several benzoanellated -, -, and fenestranes, including the parent difuso-centrotriindan 7, the parent tetrafuso-centrotetraindan 8 ("fenestrindan") as well as the tribenzo5.5.5