2-Methylanisole, 99%, Thermo Scientific Chemicals
2-Methylanisole, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Methylanisole, 99%, Thermo Scientific Chemicals

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50 g
250 g
Catalog number A13897.18
also known as A13897-18
Price (USD)/ Each
62.50
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Quantity:
50 g
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Price (USD)/ Each
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2-Methylanisole, 99%, Thermo Scientific Chemicals
Catalog numberA13897.18
Price (USD)/ Each
62.50
-
Add to cart
Chemical Identifiers
CAS578-58-5
IUPAC Name1-methoxy-2-methylbenzene
Molecular FormulaC8H10O
InChI KeyDTFKRVXLBCAIOZ-UHFFFAOYSA-N
SMILESCOC1=CC=CC=C1C
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.5%
FormLiquid
Refractive Index1.5155-1.5185 @ 20?C

The catalytic system of disubstituted aromatics was optimized for the 2-methylanisole reduction by a proper choice of the amine/Rh ratio which should be high enough to stabilize very small colloidal rhodium particles and low enough to avoid deactivation. The total synthesis of (±)-heliannuol D and its epimer has been completed in 9 steps and 12% overall yield from 2-methylanisole. The thermal activation of 2-methylanisole (60°C) by the Ir (III) complex TpMe2Ir (C6H5) 2 (N2)(1; TpMe2= hydrotris (3, 5-dimethylpyrazolyl) borate) yielded a mixture of hydride complexes. The total synthesis of the phenolic sesquiterpene mutisianthol has been accomplished in 12 steps from the readily available 2-methylanisole. The catalytic system was optimized for the 2-methylanisole reduction by a proper choice of the amine/Rh ratio which should be high enough to stabilize very small colloidal rhodium particles and low enough to avoid deactivation.

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
The catalytic system of disubstituted aromatics was optimized for the 2-methylanisole reduction by a proper choice of the amine/Rh ratio which should be high enough to stabilize very small colloidal rhodium particles and low enough to avoid deactivation. The total synthesis of (±)-heliannuol D and its epimer has been completed in 9 steps and 12% overall yield from 2-methylanisole. The thermal activation of 2-methylanisole (60°C) by the Ir (III) complex TpMe2Ir (C6H5) 2 (N2)(1; TpMe2= hydrotris (3, 5-dimethylpyrazolyl) borate) yielded a mixture of hydride complexes. The total synthesis of the phenolic sesquiterpene mutisianthol has been accomplished in 12 steps from the readily available 2-methylanisole. The catalytic system was optimized for the 2-methylanisole reduction by a proper choice of the amine/Rh ratio which should be high enough to stabilize very small colloidal rhodium particles and low enough to avoid deactivation.

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. Consuelo Pizarro,; Octavio Suárez-Iglesias,; Ignacio Medina,; Julio L. Bueno.Binary diffusion coefficients for 2,3-dimethylaniline, 2,6-dimethylaniline, 2-methylanisole, 4-methylanisole and 3-nitrotoluene in supercritical carbon dioxide. The Journal of Supercritical Fluids. 2009, 48 (1), 1-8.
  2. Kamel Nasar,; Fabienne Fache,; Marc Lemaire,; Jean-Christophe Béziat,; Michèle Besson,; Pierre Gallezot. Stereoselective reduction of disubstituted aromatics on colloidal rhodium. Journal of Molecular Catalysis. 1994, 87 (1), 107-115.