structure of 2-Amino-4-iodophenol

2-Amino-4-iodophenol

CAS No.: 99969-17-2
M. Wt: 235.02200
M. Fa: C6H6INO
InChI Key: JRCVKCSFJNERAW-UHFFFAOYSA-N

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

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

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

Physical sample testing spectrum (NMR) of 2-Amino-4-iodophenol

Retrosynthesis analysis of 2-Amino-4-iodophenol

  • Route#1

    Cas:77770-09-3
    Cas:99969-17-2
  • Route#2

    Cas:95-55-6
    Cas:99969-17-2
  • Route#3

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    Cas:99969-17-2