2-indanone
2H-inden-2-one, 1,3-dihydro-
Identification
| Name | 2-indanone |
| IUPAC | 1,3-dihydroinden-2-one |
| CAS Number | 615-13-4 |
| EINECS | 210-410-3 |
| FDA UNII | 0I79N673DE |
| Molecular Formula | C9 H8 O |
| Molecular Weight | 132.16196000 |
| MDL Number | MFCD00003792 |
| Nikkaji Number | J7.027K |
| Beilstein | 0636550 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Melting Point | 59.00 °C. @ 760.00 mm Hg |
| Boiling Point | 248.90 °C. @ 760.00 mm Hg (est) |
| Flash Point | 212.00 °F. TCC ( 100.00 °C. ) |
| logP (o/w) | 1.230 (est) |
| Soluble in | water, 5561 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | intravenous-mouse LD50 56 mg/kg |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#08390']
Safety in Use
| Category | fragrance agents |
| RIFM Fragrance Material Safety Assessment | Search |
| Recommendation for 2-indanone flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2,3-
dihydro-1H-inden-2-one
1,3-
dihydro-2H-inden-2-one
1,3-
dihydroinden-2-one
indan-2-one
2H-
inden-2-one, 1,3-dihydro-
1H-
inden-2(3H)-one
PubMed:
Bromoform activation. TiCl4-Mg-promoted CHBr2- and CBr3- transfer to a variety of aldehydes and ketones.
PubMed:
Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics.
PubMed:
Diastereoisomers of 2-benzyl-2, 3-dihydro-2-(1H-inden-2-yl)-1H-inden-1-ol: potential anti-inflammatory agents.
PubMed:
Exploring the reactivity of a coordinatively unsaturated Cp*Ru(kappa(2)-P,O) complex with small molecule substrates: application in E-H bond activation (E = H, B, and Si).
PubMed:
Calorimetric and computational study of indanones.
PubMed:
Experimental study on the thermal oxidation of 2-chlorophenol in air over the temperature range 450-900 degrees C.
PubMed:
Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3.
PubMed:
Lipoprotein mutation accelerates substrate permeability-limited toluene dioxygenase-catalyzed reaction.
PubMed:
Transition-state effects in acid-catalyzed aryl epoxide hydrolyses.
PubMed:
Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism.
PubMed:
Synthesis of 2-indanones via [4 + 1] annulation reactions of (trialkylsilyl)arylketenes.
PubMed:
Unusual reactions of 5,5-dimethyl-2-(indenyl-2)-3-pyrazolidinone with acetylenedicarboxylates
PubMed:
Pronounced differences in inhibition potency of lactone and non-lactone compounds for mouse and human coumarin 7-hydroxylases (CYP2A5 and CYP2A6).
PubMed:
New metabolites in the degradation of fluorene by Arthrobacter sp. strain F101.
PubMed:
Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase.
PubMed:
Regiospecific and stereoselective hydroxylation of 1-indanone and 2-indanone by naphthalene dioxygenase and toluene dioxygenase.
PubMed:
Metabolism and nephrotoxicity of indan in male Fischer 344 rats.
PubMed:
Gas chromatographic/mass spectrometric studies of the urinary metabolites of male rats given indan.