| Identification | Back Directory | [Name]
56-dihydroxy-indan-1- | [CAS]
124702-80-3 | [Synonyms]
56-dihydroxy-indan-1-
5,6-dihydroxy-2,3-dihydroinden-1-one
5,6-Dihydroxy-2,3-dihydro-1H-inden-1-one
1H-Inden-1-one, 2,3-dihydro-5,6-dihydroxy- | [Molecular Formula]
C9H8O3 | [MOL File]
124702-80-3.mol | [Molecular Weight]
164.16 |
| Chemical Properties | Back Directory | [Melting point ]
107-109℃ | [density ]
1.467 | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [Appearance]
Light brown to brown Solid | [InChI]
InChI=1S/C9H8O3/c10-7-2-1-5-3-8(11)9(12)4-6(5)7/h3-4,11-12H,1-2H2 | [InChIKey]
WMDAUVLSCBKCBO-UHFFFAOYSA-N | [SMILES]
C1(=O)C2=C(C=C(O)C(O)=C2)CC1 |
| Hazard Information | Back Directory | [Synthesis]
Using 5,6-dimethoxyindanone as starting material, a global demethylation reaction was carried out in dichloromethane solvent with the addition of an excess of boron tribromide (BBr3) to afford the crude product 5,6-dihydroxyindan-1-one (crude product 1) in 100% reaction yield (see Scheme 1). The crude product obtained did not require further purification and could be used directly in the subsequent reaction steps. | [References]
[1] Patent: WO2008/94896, 2008, A1. Location in patent: Page/Page column 13
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 15, p. 4308 - 4315
[3] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 20, p. 5665 - 5670
[4] Patent: WO2004/80973, 2004, A1. Location in patent: Page 133
[5] RSC Advances, 2015, vol. 5, # 34, p. 26596 - 26603 |
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