2,3-Dimethylanisole, 97%, Thermo Scientific Chemicals
2,3-Dimethylanisole, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2,3-Dimethylanisole, 97%, Thermo Scientific Chemicals

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50 g
10 g
Catalog number A19992.18
Price (USD)/ Each
159.00
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Quantity:
50 g
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Price (USD)/ Each
159.00
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2,3-Dimethylanisole, 97%, Thermo Scientific Chemicals
Catalog numberA19992.18
Price (USD)/ Each
159.00
-
Add to cart
Chemical Identifiers
CAS2944-49-2
IUPAC Name1-methoxy-2,3-dimethylbenzene
Molecular FormulaC9H12O
InChI KeyBLMBNEVGYRXFNA-UHFFFAOYSA-N
SMILESCOC1=CC=CC(C)=C1C
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
Refractive Index1.5190-1.5240 @ 20?C
2,3-Dimethylanisole is used as starting reagent in the synthesis of biphenyl-indanone A, a positive allosteric modulator of the metabotropic glutamate receptor subtype 2. It can be used to produce 2-methoxy-6-methyl-benzaldehyde by heating.

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
2,3-Dimethylanisole is used as starting reagent in the synthesis of biphenyl-indanone A, a positive allosteric modulator of the metabotropic glutamate receptor subtype 2. It can be used to produce 2-methoxy-6-methyl-benzaldehyde by heating.

Solubility
Not miscible or difficult to mix in water.

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

General References:

  1. Goldberg Y, et al. Highly regioselective bromination of 2, 3-dimethylanisole with N-bromosuccinimide.J. Org. Chem.1992,57(23), 6374-6376.
  2. Ruggero Galici, et al. Biphenyl-indanone A, a positive allosteric modulator of the metabotropic glutamate receptor subtype 2, has antipsychotic- and anxiolytic-like effects in mice.J Pharmacol Exp Ther.2006,318(1),173-185.
  3. Methyl groups o- or p- to alkoxy groups can be selectively oxidized to the aldehyde by potassium peroxydisulfate in the presence of Cu(II): Synthesis, 723 (1987).