122911-57-3

Basic information

• Product Name: 2-(2-styryl)indane-1,3-dione
• Synonyms: 2-(2-styryl)indane-1,3-dione
• CAS NO: 122911-57-3
• Molecular Weight: 248.281
• Mol File: 122911-57-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(2-styryl)indane-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-styryl)indane-1,3-dione(122911-57-3)
• EPA Substance Registry System: 2-(2-styryl)indane-1,3-dione(122911-57-3)

Safety Data

• Hazardous Substances Data: 122911-57-3(Hazardous Substances Data)

Upstream product

• 35106-82-2 2-vinylbenzylalcohol 
• 28272-96-0 2-vinylbenzaldehyde 
• 87-41-2 2-benzofuran-1(3H)-one 
• 90537-01-2 2-dibromomethyl-benzoic acid methyl ester 
• 27326-44-9 methyl o-vinylbenzoate 
• 89-71-4 2-Methyl-benzoic acid methyl ester 
• 4122-56-9 methyl o-formylbenzoate 

Downstream Products

• 136054-95-0 Methanesulfonic acid 2-[2-(3-methoxy-1-oxo-1H-inden-2-yl)-phenyl]-ethyl ester 
• 136054-96-1 2-(ω-bromoethylphenyl)-3-methoxyindenone 
• 136054-94-9 2-(ω-hydroxyethylphenyl)-3-methoxyindenone 
• 136054-93-8 3-methoxy-2-(2-styryl)indenone 
• 155129-53-6 2-Bromo-2-(2-vinyl-phenyl)-indan-1,3-dione 
• 155129-52-5 2-Chloro-2-(2-vinyl-phenyl)-indan-1,3-dione 

Relevant articles and documents

Manganese(III) Mediated Synthesis of SpiroNonane System Present in Fredericamycin A

A convenient approach for constructing the spirononane system of Fredericamycin A has been demonstrated using a manganese(III) based oxidative free radical cyclisation.

Regioselective Free Radical Cyclization: a General Method for the Synthesis of the Spirononane System of Fredericamycin A

Introduction of a halogen atom at the middle carbon atom of cyclic 1,3-diketones is described.A convenient approach for constructing the spirononane system of fredericamycin A has been demonstrated by halogen transfer during radical cyclization follo

Palladium(II)-mediated Synthesis of Spirononane System Present in Fredericamycin A

A convenient approach for the construction of spirononane system present in fredericamycin A (1) has been achieved utilizing Pd(II) acetate mediated cyclisation of the 1,3-indanedione intermediate (10).