2-Methyl-indanone
Names
[ CAS No. ]:
17496-14-9
[ Name ]:
2-Methyl-indanone
[Synonym ]:
2-Methylindan-1-One
2-methyl-2,3-dihydroinden-1-one
1H-Inden-1-one, 2,3-dihydro-2-methyl-
2-Methyl-indanone
2-methyl-2,3-dihydro-1H-inden-1-one
2-Methyl-1-indanone
MFCD00192303
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
238.4±10.0 °C at 760 mmHg
[ Molecular Formula ]:
C10H10O
[ Molecular Weight ]:
146.186
[ Flash Point ]:
94.4±14.0 °C
[ Exact Mass ]:
146.073166
[ PSA ]:
17.07000
[ LogP ]:
2.59
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.554
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;Xn: Harmful;
[ Risk Phrases ]:
R22
[ Safety Phrases ]:
23-26-36/37/39-36
[ RIDADR ]:
NONH for all modes of transport
[ 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. Org. Chem. 72(24) , 9372-5, (2007)
A convenient access to substituted allyl enol carbonates was established through the reaction of ketone enolates with the complex of allyl 1H-imidazole-1-carboxylates and boron trifluoride etherate.
Recent advances in enzymatic and chemical deracemisation of racemic compounds.Chem. Soc. Rev. 42(24) , 9268-9282, (2013)
Deracemisation of racemic compounds is still the most important strategy to produce optically pure compounds despite many recent advances in asymmetric synthesis. Especially deracemisation approaches ...
Amino alcohol-mediated enantioselective syntheses of α-substituted indanones and tetralones, ammonium enolates as key intermediates. Muzart J.Tetrahedron Asymmetry 25(9) , 697-704, (2014)