ChemicalBook--->CAS DataBase List--->124702-80-3

124702-80-3

124702-80-3 Structure

124702-80-3 Structure
IdentificationBack 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 PropertiesBack 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
Spectrum DetailBack Directory
[Spectrum Detail]

56-dihydroxy-indan-1-(124702-80-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

5,6-Dimethoxy-1-indanone

2107-69-9

56-dihydroxy-indan-1-

124702-80-3

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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