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Thermo Scientific Chemicals
2,6-Dimethylaniline, 99%
CAS: 87-62-7 | C8H11N | 121.18 g/mol
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Catalog number A14512.36
also known as A14512-36
Price (EUR)
66,70
Each
Quantity:
500 g
Price (EUR)
66,70
Each
Chemical Identifiers
CAS87-62-7
IUPAC Name2,6-dimethylaniline
Molecular FormulaC8H11N
InChI KeyUFFBMTHBGFGIHF-UHFFFAOYSA-N
SMILESCC1=CC=CC(C)=C1N
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to white to yellow to red to red-brown
FormLiquid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Refractive Index1.5590-1.5620 @ 20°C
2,6-Dimethylaniline is used in pharmaceuticals, as dye intermediates and in organic synthesis. It is also used in the production of antioxidants, agricultural, pharmaceutical, rubber chemicals and other target organic molecules.
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
2,6-Dimethylaniline is used in pharmaceuticals, as dye intermediates and in organic synthesis. It is also used in the production of antioxidants, agricultural, pharmaceutical, rubber chemicals and other target organic molecules.
Solubility
Slightly miscible with water. Miscible with ethanol and diethyl ether.
Notes
It is sensitive to air and light. Incompatible withacids, acid chlorides, acid anhydrides, oxidizing agents, chloroformates and halogens.
2,6-Dimethylaniline is used in pharmaceuticals, as dye intermediates and in organic synthesis. It is also used in the production of antioxidants, agricultural, pharmaceutical, rubber chemicals and other target organic molecules.
Solubility
Slightly miscible with water. Miscible with ethanol and diethyl ether.
Notes
It is sensitive to air and light. Incompatible withacids, acid chlorides, acid anhydrides, oxidizing agents, chloroformates and halogens.
RUO – Research Use Only
General References:
- Hindered aromatic amines do not form imines by direct reaction with benzophenones. An indirect route involves formation of the imine with an aldehyde, introduction of the second aryl group by 1,2-addition of the aryllithium and dehydrogenation of the resulting secondary amine with DDQ: J. Org. Chem., 54, 2464 (1989).
- Huang, W. C.; Lin, Y. C. ; Tzeng, W. B. Mass-analyzed threshold ionization spectroscopy of 2,6-dimethylaniline, 2,6-dimethylaniline-NHD, and 2,6-dimethylaniline-ND2. Chem. Phys. Lett. 2012, 551, 50-53.
- Ting, W-P.; Huang, Y-H.; Lu, M-C. Oxidation of 2,6-dimethylaniline by the Fenton, electro-Fenton and photoelectro-Fenton processes. J. Environ. Sci. Health, Part A 2011, 46 (10), 1085-1091.
- Gockel, S. N.; Hull, K. L. Chloroform as a Carbon Monoxide Precursor: In or Ex Situ Generation of CO for Pd-Catalyzed Aminocarbonylations. Org. Lett. 2015, 17 (13), 3236-3239.
- Yao, Q.; Wang, Z.; Zhang, Y.; Liu, X.; Lin, L.; Feng, X. N,N'-Dioxide/Gadolinium(III)-Catalyzed Asymmetric Conjugate Addition of Nitroalkanes to α, β-Unsaturated Pyrazolamides. J. Org. Chem. 2015, 80 (11), 5704-5712.