CAS 83863-33-6
:5-Iodo-2-methylaniline
Description:
5-Iodo-2-methylaniline is an organic compound characterized by the presence of an aniline structure, which consists of an amino group (-NH2) attached to a benzene ring. In this compound, a methyl group (-CH3) and an iodine atom (I) are substituted at the 2 and 5 positions of the benzene ring, respectively. This substitution pattern influences its chemical reactivity and physical properties. The compound typically appears as a solid or liquid, depending on the temperature, and is known for its potential applications in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. It is important to handle 5-iodo-2-methylaniline with care, as it may pose health risks, including skin and respiratory irritation. Additionally, its iodine content can impart unique reactivity, making it useful in various chemical transformations. As with many organic compounds, proper safety protocols should be followed when working with this substance in a laboratory setting.
Formula:C7H8IN
InChI:InChI=1/C7H8IN/c1-5-2-3-6(8)4-7(5)9/h2-4H,9H2,1H3
InChI key:InChIKey=IOEHXNCBPIBDBZ-UHFFFAOYSA-N
SMILES:NC1=C(C)C=CC(I)=C1
Synonyms:- 2-Amino-4-iodotoluene
- 3-Iodo-6-methylaniline
- 5-Iodo-2-Methyl-Phenylamine
- 5-Iodo-2-methylbenzenamine
- 5-Iodo-o-toluidine
- 5-Iodo-o-toluidine (NH2=1)
- Benzenamine, 5-iodo-2-methyl-
- 5-Iodo-2-methylaniline
- TIMTEC-BB SBB007547
- 2-Amino-4-iodotoluene~5-Iodo-o-toluidine
- 2-Methyl-5-iodoaniline
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Found 5 products.
5-Iodo-2-methylaniline
CAS:5-Iodo-2-methylanilineFormula:C7H8INPurity:≥95%Color and Shape: brown powderMolecular weight:233.05g/mol5-Iodo-2-methylaniline
CAS:Formula:C7H8INPurity:>98.0%(GC)(T)Color and Shape:Light yellow to Brown to Dark green powder to crystalMolecular weight:233.055-Iodo-2-methylaniline
CAS:<p>5-Iodo-2-methylaniline is an organic compound that belongs to the class of safranines. It has an arrayed, spectra, and fluorescence spectrum. 5-Iodo-2-methylaniline is synthesized from 2-iodoaniline and formaldehyde in the presence of a reducing agent such as sodium borohydride or sodium triacetoxyborohydride. The electron transfer process can be monitored by changes in the absorbance of the solution, which are related to reduction potentials and electron transfer rates. Safranin is reduced by 5-iodo-2-methylaniline to produce a red color with a maximum absorption at about 600 nm. Safranin is oxidized back to its original state by adding hydrogen peroxide to produce a colorless product with a maximum absorption at about 620 nm.</p>Formula:C7H8INPurity:Min. 95%Color and Shape:PowderMolecular weight:233.05 g/mol




