104079-37-0

Basic information

• Product Name: 1H-Indene-2-acetaldehyde, 2,3-dihydro-1,3-dioxo-2-phenyl-
• CAS NO: 104079-37-0
• Molecular Formula: C17H12O3
• Molecular Weight: 264.28
• Mol File: 104079-37-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indene-2-acetaldehyde, 2,3-dihydro-1,3-dioxo-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indene-2-acetaldehyde, 2,3-dihydro-1,3-dioxo-2-phenyl-(104079-37-0)
• EPA Substance Registry System: 1H-Indene-2-acetaldehyde, 2,3-dihydro-1,3-dioxo-2-phenyl-(104079-37-0)

Safety Data

• Hazardous Substances Data: 104079-37-0(Hazardous Substances Data)

Upstream product

• 94802-89-8 2-allyl-2-phenylindene-1,3(2H)-dione 
• 876291-59-7 4-fluoro-2-phenylindan-1,3-dione 
• 876291-60-0 2-allyl-4-fluoro-2-phenyl-indan-1,3-dione 
• 652-39-1 3-fluorophthalic anhydride 
• 1583-67-1 3-fluorophthalic acid 
• 83-12-5 phenindione 
• 85-44-9 phthalic anhydride 

Downstream Products

• 104079-39-2 2-(2,2-Bis-ethylsulfanyl-ethyl)-2-phenyl-indan-1,3-dione 
• 106116-61-4 2,3-Dihydro-1,3-diphenyl-7H-benzanthracen-7-on 

Relevant articles and documents

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.

An Unusual Synthesis of a Dihydrobenzanthrone

The reaction of the aldehyde 1 with aluminium trichloride in benzene affords the dihydrobenzanthrone 2.The structure is confirmed by an X-ray analysis.Dehydrogenation of 2 yields the benzanthrone 3, which shows a greenish yellow fluorescence.According to the 1H-NMR and mass spectra, the deuterated products 5 and 6 are formed, when the key reaction is carried out in benzene.