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Thermo Scientific Chemicals
1-Indanone, 99+%
CAS: 83-33-0 | C9H8O | 132.162 g/mol
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Catalog number A11056.14
also known as A11056-14
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Quantity:
25 g
Chemical Identifiers
CAS83-33-0
IUPAC Name2,3-dihydro-1H-inden-1-one
Molecular FormulaC9H8O
InChI KeyQNXSIUBBGPHDDE-UHFFFAOYSA-N
SMILESO=C1CCC2=CC=CC=C12
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Specifications
Specification Sheet
Specification SheetAssay (GC)≥99.0%
FormCrystals or powder or crystalline powder or fused solid or chunks or lumps
Appearance (Color)White to pale yellow or pale brown
Solution Test2.5% w/v solution in ethanol, 99.5% will be transparent to very faintly turbid by JIS K 8001 5.2
1-Indanone is an oxidation product of indan, a component of fuels, solvents and varnishes. 1-Indanone is also a metabolite of Thalidomide that has been shown to inhibit the attachment of tumor cells to concanavalin A coated plastic surfaces.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1-Indanone is an oxidation product of indan, a component of fuels, solvents and varnishes. 1-Indanone is also a metabolite of Thalidomide that has been shown to inhibit the attachment of tumor cells to concanavalin A coated plastic surfaces.
Solubility
Soluble in water (6.5 g/L at 20°C).
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
1-Indanone is an oxidation product of indan, a component of fuels, solvents and varnishes. 1-Indanone is also a metabolite of Thalidomide that has been shown to inhibit the attachment of tumor cells to concanavalin A coated plastic surfaces.
Solubility
Soluble in water (6.5 g/L at 20°C).
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- S.M.Resnick; D.S.Torok; K.Lee; J.M.Brand; D.T.Gibson. Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase. Appl. Environ. Microbiol. 1994, 60,(9), 3323-3328.
- M.E.Long; E.C.Lim. Phosphorescence of 1-indanone and related compounds. Chemical Physics Letters. 1973, 20,(5), 413-418.
- Can be carboxylated at the 2-position in the presence of diphenylcarbodiimide: Chem. Lett., 39 (1990):