Basic information Safety Supplier Related

2-Methylindene

Basic information Safety Supplier Related

2-Methylindene Basic information

Product Name:
2-Methylindene
Synonyms:
  • 2-METHYL-1H-INDENE
  • 2-METHYL-1H-INDENE 98+%
  • 2-METHYLINDENE
  • 2-Methylindene 98%
  • 1H-Indene, 2-methyl-
  • Indene, 2-methyl-
  • indene,2-methyl-
CAS:
2177-47-1
MF:
C10H10
MW:
130.19
Product Categories:
  • Arenes
  • Building Blocks
  • Organic Building Blocks
  • Indanone & Indene
Mol File:
2177-47-1.mol
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2-Methylindene Chemical Properties

Melting point:
80°C
Boiling point:
45 °C0.2 mm Hg(lit.)
Density 
0.971 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.567(lit.)
Flash point:
169 °F
storage temp. 
Sealed in dry,Room Temperature
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C10H10/c1-8-6-9-4-2-3-5-10(9)7-8/h2-6H,7H2,1H3
InChIKey
YSAXEHWHSLANOM-UHFFFAOYSA-N
SMILES
C1C2=C(C=CC=C2)C=C1C
CAS DataBase Reference
2177-47-1(CAS DataBase Reference)
NIST Chemistry Reference
2-Methylindene(2177-47-1)
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Safety Information

WGK Germany 
3

MSDS

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2-Methylindene Usage And Synthesis

Chemical Properties

transparent to yellow liquid

Synthesis

17496-14-9

2177-47-1

The general procedure for the synthesis of 2-methylindene (6) from 2-methylindan-1-one (5) was as follows: 5.0 g (34 mmol) of 2-methyl-1-indanone (5) was reacted with 1.94 g (51 mmol) of NaBH4 in a reduction reaction according to the method of Example G. Subsequently, the unpurified alcohol was further reacted in 100 g of toluene catalyzed by 0.2 g of p-toluenesulfonic acid at 80 °C. The reaction mixture was purified by column chromatography on 100 g silica gel with hexane/dichloromethane (9:1) as eluent to give 3.68 g (82% yield) of the target product 2-methylindene (6). The product was characterized by 1H-NMR (100 MHz, CDCl3): δ 7.2 (4H, m), 6.45 (1H, m), 3.25 (2H, m), 2.1 (3H, m). Mass spectrometry analysis showed a molecular ion peak of 130 M+ and a cleavage pattern as expected.

References

[1] Journal of Chemical Research, 2010, # 6, p. 325 - 329
[2] Journal of Organic Chemistry, 1980, vol. 45, # 23, p. 4564 - 4572
[3] Journal of Organic Chemistry, 1984, vol. 49, # 22, p. 4226 - 4237
[4] Journal of Organic Chemistry, 1982, vol. 47, # 6, p. 1051 - 1058
[5] Collection of Czechoslovak Chemical Communications, 1983, vol. 48, # 1, p. 60 - 70

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