2-Amino-4-iodophenol
Names and Identifiers of 2-Amino-4-iodophenol
CAS Number |
99969-17-2 |
|---|---|
EC Number |
812-757-1 |
MDL Number |
MFCD14705890 |
IUPAC Name |
2-amino-4-iodophenol |
InChI |
InChI=1S/C6H6INO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,8H2 |
InChIKey |
JRCVKCSFJNERAW-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC(=C(C=C1I)N)O |
UNSPSC Code |
12352100 |
Physical and chemical properties of 2-Amino-4-iodophenol
Exact Mass |
234.94900 |
|---|---|
LogP |
2.16020 |
Melting Point |
139°C |
Molecular Formula |
C6H6INO |
Molecular Weight |
235.02200 |
PSA |
46.25000 |
Storage condition |
under inert gas (nitrogen or Argon) at 2–8 °C |
Safety Information of 2-Amino-4-iodophenol
Applications of 2-Amino-4-iodophenol
2-Amino-4-iodophenol has diverse applications across several fields:
- Chemical Synthesis: It serves as an intermediate in synthesizing more complex organic molecules.
- Biological Research: The compound is used in studies involving enzyme interactions and as a precursor for biologically active compounds.
- Industrial Use: It finds utility in producing dyes, pigments, and other industrial chemicals due to its unique reactivity profile.
Interaction Studies of 2-Amino-4-iodophenol
Research on 2-Amino-4-iodophenol has highlighted its potential interactions with various molecular targets. The amino group facilitates hydrogen bonding, while the iodine atom can participate in substitution reactions that affect biological pathways. These properties make it a useful tool for investigating biochemical mechanisms and developing new therapeutic agents.
Biological Activity of 2-Amino-4-iodophenol
The biological activity of 2-Amino-4-iodophenol has been explored in various studies. Its structure allows it to interact with biological molecules, potentially influencing enzyme activities and other biochemical pathways. The amino group can engage in hydrogen bonding, while the iodine atom may facilitate the formation of reactive intermediates. This compound has applications in studying enzyme interactions and developing biologically active molecules.
Physical sample testing spectrum (NMR) of 2-Amino-4-iodophenol
