94802-89-8

Basic information

• Product Name: 2-allyl-2-phenylindene-1,3(2H)-dione
• Synonyms: 2-allyl-2-phenylindene-1,3(2H)-dione
• CAS NO: 94802-89-8
• Molecular Weight: 262.308
• Mol File: 94802-89-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-allyl-2-phenylindene-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-allyl-2-phenylindene-1,3(2H)-dione(94802-89-8)
• EPA Substance Registry System: 2-allyl-2-phenylindene-1,3(2H)-dione(94802-89-8)

Safety Data

• Hazardous Substances Data: 94802-89-8(Hazardous Substances Data)

Upstream product

• 83-12-5 phenindione 
• 107-18-6 allyl alcohol 
• 85-44-9 phthalic anhydride 
• 1583-67-1 3-fluorophthalic acid 
• 652-39-1 3-fluorophthalic anhydride 
• 876291-59-7 4-fluoro-2-phenylindan-1,3-dione 
• 876291-60-0 2-allyl-4-fluoro-2-phenyl-indan-1,3-dione 
• 106-95-6 allyl bromide 

Downstream Products

• 104079-39-2 2-(2,2-Bis-ethylsulfanyl-ethyl)-2-phenyl-indan-1,3-dione 
• 104079-37-0 2-(Formylmethyl)-2-phenyl-1,3-indandion 

Relevant articles and documents

Domino Michael-seleno Pummerer type reaction (additive seleno Pummerer reaction)

Domino Michael-seleno Pummerer type reaction (additive seleno Pummerer type rearrangement) has been realised by the reaction of 1,3-dicarbonyl compounds with vinyl selenoxides in the presence of amine and chlorosilane. The Royal Society of Chemistry 2000.

Sarcosine based indandione hGlyT1 inhibitors

A series of sarcosine based indandione hGlyT1 inhibitors has been developed. Optimization of substitution around the indandione and sarcosine moieties has led to highly potent inhibitors at hGlyT1, which show selectivity over a number of other receptors.

SYNTHESIS OF SPIROCYCLIC DIKETONES RELATED TO FREDERICAMYCIN A

An intramolecular Friedel-Crafts type reaction of the thioacetals 7a and 7b is the key step in a simple synthesis of the diketones 2a and 2b.