2-Indanone
Names
[ CAS No. ]:
615-13-4
[ Name ]:
2-Indanone
[Synonym ]:
EINECS 210-410-3
MFCD00003792
1,3-dihydroinden-2-one
2-Indanone
2-oxo-2,3-dihydro-1H-indene
2H-Inden-2-one, 1,3-dihydro-
2H-Inden-2-one,1,3-dihydro
2,3-dihydro-1H-inden-2-one
1,3-Dihydro-2H-inden-2-one
indan-2-one
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
248.9±29.0 °C at 760 mmHg
[ Melting Point ]:
51-54 °C(lit.)
[ Molecular Formula ]:
C9H8O
[ Molecular Weight ]:
132.159
[ Flash Point ]:
100.0±0.0 °C
[ Exact Mass ]:
132.057510
[ PSA ]:
17.07000
[ LogP ]:
1.23
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.585
[ Storage condition ]:
2-8°C
[ Water Solubility ]:
insoluble
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- NK7535500
- CHEMICAL NAME :
- 2-Indanone
- CAS REGISTRY NUMBER :
- 615-13-4
- BEILSTEIN REFERENCE NO. :
- 0636550
- LAST UPDATED :
- 199709
- DATA ITEMS CITED :
- 2
- MOLECULAR FORMULA :
- C9-H8-O
- MOLECULAR WEIGHT :
- 132.17
- WISWESSER LINE NOTATION :
- L56 CVT&J
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 56 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#08390
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
NK7535500
[ Packaging Group ]:
II; III
[ Hazard Class ]:
4.1
[ HS Code ]:
2914399090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2914399090
[ Summary ]:
2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%
Articles
J. Med. Chem. 48 , 3808-15, (2005)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-ac...
Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics.J. Org. Chem. 76(13) , 5335-45, (2011)
Indene-fused porphyrins have been synthesized starting from 2-indanone. Knorr-type reaction of oximes derived from benzyl or tert-butyl acetoacetate with 2-indanone and zinc dust in propionic acid gav...
Bromoform activation. TiCl4-Mg-promoted CHBr2- and CBr3- transfer to a variety of aldehydes and ketones.Org. Lett. 15(22) , 5802-5, (2013)
TiCl4-Mg can mediate addition of CHBr3 to a variety of aldehydes and ketones to form dibromomethyl carbinols and also be used to effect CBr3 transfer to carbonyl groups to form tribromomethyl carbinol...