| Identification | Back Directory | [Name]
2-METHYL-1-INDANONE | [CAS]
17496-14-9 | [Synonyms]
2-METHYL-INDANONE
2-METHYL-1-INDANONE
2-METHYLINDAN-1-ONE
2-METHYL-1-INDANONE 97%
(R,S)-2-Methyl-indan-1-one
2-methyl-2,3-dihydroinden-1-one
2,3-Dihydro-2-methyl-1H-inden-1-one
2-Methyl-2,3-dihydro-1H-inden-1-one
2,3-Dihydro-2-methyl-1H-inden-1-one, 1-Oxo-2-methylindane | [Molecular Formula]
C10H10O | [MDL Number]
MFCD00192303 | [MOL File]
17496-14-9.mol | [Molecular Weight]
146.19 |
| Chemical Properties | Back Directory | [Appearance]
Pale yellow liquid | [Melting point ]
47-47.5 °C | [Boiling point ]
93-95 °C4 mm Hg(lit.)
| [density ]
1.064 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.555(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [form ]
liquid | [color ]
Yellow | [InChI]
InChI=1S/C10H10O/c1-7-6-8-4-2-3-5-9(8)10(7)11/h2-5,7H,6H2,1H3 | [InChIKey]
BEKNOGMQVKBMQN-UHFFFAOYSA-N | [SMILES]
C1(=O)C2=C(C=CC=C2)CC1C |
| Hazard Information | Back Directory | [Chemical Properties]
Pale yellow liquid | [Uses]
2-Methyl-1-indanone may be used as a starting material in the synthesis of β-benzocycloalkenone. It may be used in the synthesis of the following:
- cyclohex-2-en-1-yl 2-methyl-1H-inden-3-yl carbonate
- 2-hydroxy-2-methyl-1-indanone
- O-alkoxycarbonylation of lithium enolates
| [Synthesis Reference(s)]
The Journal of Organic Chemistry, 46, p. 3758, 1981 DOI: 10.1021/jo00331a046
Tetrahedron Letters, 29, p. 2183, 1988 DOI: 10.1016/S0040-4039(00)86705-2 | [General Description]
2-Methyl-1-indanone, a α-benzocycloalkenone, is a derivative of 1-indanone. Its synthesis has been reported. The enzymatic dynamic kinetic resolution (DKR) of racemic 2-methyl-1-indanone has been studied. The asymmetric α-arylation and hydroxymethylation of 2-methyl-1-indanone has been reported. It participated in the synthesis of 2-methyl-6-carboxyazulene. |
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