CAS 66416-72-6
:4-bromo-2-iodoaniline
Description:
4-Bromo-2-iodoaniline is an organic compound characterized by the presence of both bromine and iodine substituents on an aniline structure. It features a benzene ring with an amino group (-NH2) attached, along with a bromine atom at the para position (4-position) and an iodine atom at the ortho position (2-position) relative to the amino group. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. It is known for its reactivity, particularly in electrophilic aromatic substitution reactions, due to the electron-donating nature of the amino group and the electron-withdrawing effects of the halogen substituents. 4-Bromo-2-iodoaniline can be utilized in various applications, including organic synthesis, pharmaceuticals, and as an intermediate in the production of dyes and pigments. Safety precautions should be observed when handling this compound, as both bromine and iodine are hazardous substances.
Formula:C6H5BrIN
InChI:InChI=1/C6H5BrIN/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2
InChI key:InChIKey=HHTYEQWCHQEJNV-UHFFFAOYSA-N
SMILES:IC1=C(N)C=CC(Br)=C1
Synonyms:- 2-Iodo-4-bromoaniline
- 4-Bromo-2-iodobenzenamine
- 4-Bromo-2-iodophenylamine
- Benzenamine, 4-Bromo-2-Iodo-
- Zr Bi De [Wln]
- 4-Bromo-2-iodoaniline
- AKOS BB-7878
- 4-Bromo-2-iodoaniline >
- 4-bromo-2-iodo-benzenamine
- 4-BROMO-2-IODOANILINE ISO 9001:2015 REACH
- 4-BROMO-2-IODO-PHENYLAMINE
- 4-Bromo-2-iodoaniline 97%
- ASISCHEM T54343
- See more synonyms
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Found 5 products.
4-Bromo-2-iodoaniline
CAS:<p>4-Bromo-2-iodoaniline</p>Formula:C6H5BrINPurity:≥95%Color and Shape: very dark grey crystalline solidMolecular weight:297.92g/mol4-Bromo-2-iodoaniline
CAS:Formula:C6H5BrINPurity:>97.0%(GC)(T)Color and Shape:White to Gray to Red powder to crystalMolecular weight:297.924-Bromo-2-iodoaniline
CAS:<p>4-Bromo-2-iodoaniline is a peroxide with a hydrophobic nature. It is an intermediate in the synthesis of the herbicide Arbidol and the pharmaceuticals 4-Bromo-2,6-dinitroaniline and aminopyridine. Oxidation of 4-bromo-2-iodoaniline can be accomplished by halogenation with hydrogen peroxide or trifluoroacetic acid. The halides are then replaced by chlorine to form bromochlorodianisole, which is an intermediate for the synthesis of aminopyridine. Other functional groups that react with 4-bromo-2-iodoaniline are amines, arbidol, chloride, and potassium thioacetate. Fluorescent tests indicate that this compound has a strong absorption at 360 nm and emission at 420 nm. This reaction is also used as a virus detection test due to its</p>Formula:C6H5BrINPurity:Min. 95%Color and Shape:PowderMolecular weight:297.92 g/mol




