2,6-Dibromo-4-methylaniline, 98+%
2,6-Dibromo-4-methylaniline, 98+%
2,6-Dibromo-4-methylaniline, 98+%
2,6-Dibromo-4-methylaniline, 98+%
Thermo Scientific Chemicals

2,6-Dibromo-4-methylaniline, 98+%

CAS: 6968-24-7 | C7H7Br2N | 264.948 g/mol
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100 g
Catalog number A17184.22
also known as A17184-22
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Quantity:
100 g
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Price (EUR)
124,00
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Chemical Identifiers
CAS6968-24-7
IUPAC Name2,6-dibromo-4-methylaniline
Molecular FormulaC7H7Br2N
InChI KeyATDIROHVRVQMRO-UHFFFAOYSA-N
SMILESCC1=CC(Br)=C(N)C(Br)=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Cream
Assay (GC)≥98.0%
Melting Point (clear melt)70.5-76.5?C
FormPowder
2,6-Dibromo-4-methylaniline is used as coupling reagent in spectrophotometric determination of carbaryl in various environmental samples. It was also in preparation of 2-bromo-6-iodo-4-methylaniline. 2,6-Dibromo-4-methylaniline undergoes Suzuki-coupling reaction with 2-dihydroxyboryl-3-methyl-2-cyclopenten-1-one during synthesis of the dinuclear dichlorotitanium complexes. 2,6-Dibromo-4-methylaniline is also used as an intermediate for the synthesis of pharmaceutucals, agrochemicals, dyes and other organic chemicals.

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-Dibromo-4-methylaniline is used as coupling reagent in spectrophotometric determination of carbaryl in various environmental samples. It was also in preparation of 2-bromo-6-iodo-4-methylaniline. 2,6-Dibromo-4-methylaniline undergoes Suzuki-coupling reaction with 2-dihydroxyboryl-3-methyl-2-cyclopenten-1-one during synthesis of the dinuclear dichlorotitanium complexes. 2,6-Dibromo-4-methylaniline is also used as an intermediate for the synthesis of pharmaceutucals, agrochemicals, dyes and other organic chemicals.

Solubility
Insoluble in water.

Notes
Stable under ordinary conditions.
RUO – Research Use Only

General References:

  1. RR Holmes.; RP Bayer. A Simple Method for the Direct Oxidation of Aromatic Amines to Nitroso Compounds1. J. Am. Chem. Soc. 196082 (13), 3454-3456.
  2. HK Lee.; TM Rana. Microwave-assisted parallel synthesis of a 4, 6-diamino-2, 2-dimethyl-1, 2-dihydro-1-phenyl-s-triazine library. J. Comb. Chem.20046 (4), 504-508.