163228
2-Methyl-1-tetralone
98%
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About This Item
Empirical Formula (Hill Notation):
C11H12O
CAS Number:
Molecular Weight:
160.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-461-8
MDL number:
Assay:
98%
Form:
liquid
Product Name
2-Methyl-1-tetralone, 98%
InChI key
GANIBVZSZGNMNB-UHFFFAOYSA-N
InChI
1S/C11H12O/c1-8-6-7-9-4-2-3-5-10(9)11(8)12/h2-5,8H,6-7H2,1H3
SMILES string
CC1CCc2ccccc2C1=O
assay
98%
form
liquid
refractive index
n20/D 1.5535 (lit.)
bp
127-131 °C/12 mmHg (lit.)
density
1.057 g/mL at 25 °C (lit.)
functional group
ketone
Quality Level
Related Categories
Application
2-Methyl-1-tetralone was used in enantioselective separation of indan, tetralin and benzosuberan derivatives in the presence of chiral additives by capillary electrophoresis.
General description
2-Methyl-1-tetralone undergoes enantioselective hydrogenation catalyzed by 1,4-diamine-ruthenium(II) complexes.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Chiral separations of indan, tetralin and benzosuberan derivatives by capillary electrophoresis.
Gahm K-H, et al.
Journal of Chromatography A, 793(1), 135-143 (1998)
Takeshi Ohkuma et al.
Organic letters, 6(16), 2681-2683 (2004-07-30)
A combined system of a RuCl(2)(binap)(1,4-diamine) complex and t-C(4)H(9)OK in i-C(3)H(7)OH catalyzes enantioselective hydrogenation of various 1-tetralone derivatives and some methylated 2-cyclohexenones. Hydrogenation of 2-methyl-1-tetralone under dynamic kinetic resolution gives the cis alcohol with high ee. [reaction: see text]
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