2-Methyl-1-tetralone, 97%, Thermo Scientific Chemicals
2-Methyl-1-tetralone, 97%, Thermo Scientific Chemicals
2-Methyl-1-tetralone, 97%, Thermo Scientific Chemicals
2-Methyl-1-tetralone, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Methyl-1-tetralone, 97%, Thermo Scientific Chemicals

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Catalog NumberQuantity
H31865.03
also known as H31865-03
1 g
Catalog number H31865.03
also known as H31865-03
Price (EUR)
64,70
Each
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Quantity:
1 g
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Price (EUR)
64,70
Each
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Chemical Identifiers
CAS1590-08-5
IUPAC Name2-methyl-1,2,3,4-tetrahydronaphthalen-1-one
Molecular FormulaC11H12O
InChI KeyGANIBVZSZGNMNB-UHFFFAOYNA-N
SMILESCC1CCC2=CC=CC=C2C1=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥96.0%
Refractive Index1.5505-1.5545 @ 20°C
Methylation of 1-tetralone followed by the subsequent dehydrogenation of 2-methyl-1-tetralone in the presence of Pd/C catalyst also has been reported.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Methylation of 1-tetralone followed by the subsequent dehydrogenation of 2-methyl-1-tetralone in the presence of Pd/C catalyst also has been reported.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Jason Eames,; Neluka Weerasooriya. Investigations into the enantioselective protonation of enolates derived from 2-methyl-1-tetralone using a chiral diamine ligand . Tetrahedron Letters. 2000, 41(4), 521-523.
  2. Ewan Boyd,; Gregory S. Coumbarides,; Jason Eamesb,; Alastair Hay,; Ray V.H. Jones,; Rachel A. Stensonc,; Michael J. Suggate. Reversal of enantioselectivity on protonation of enol(ate)s derived from 2-methyl-1-tetralone using C2-symmetric sulfonamides. Tetrahedron Letters. 2004, 45 (51), 9465-9468.