structure of 6-Amino-2-fluoro-3-iodobenzonitrile

6-Amino-2-fluoro-3-iodobenzonitrile

CAS No.: 1000577-82-1
M. Wt: 262.02300
M. Fa: C7H4FIN2
InChI Key: NXYRGTVCZLTGEZ-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 6-Amino-2-fluoro-3-iodobenzonitrile

CAS Number

1000577-82-1

EC Number

825-483-2

MDL Number

MFCD09800813

IUPAC Name

6-amino-2-fluoro-3-iodobenzonitrile

InChI

InChI=1S/C7H4FIN2/c8-7-4(3-10)6(11)2-1-5(7)9/h1-2H,11H2

InChIKey

NXYRGTVCZLTGEZ-UHFFFAOYSA-N

Canonical SMILES

C1=CC(=C(C(=C1N)C#N)F)I

UNSPSC Code

12352100

Physical and chemical properties of 6-Amino-2-fluoro-3-iodobenzonitrile

Exact Mass

261.94000

LogP

2.46538

Molecular Formula

C7H4FIN2

Molecular Weight

262.02300

PSA

49.81000

Safety Information of 6-Amino-2-fluoro-3-iodobenzonitrile

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 6-Amino-2-fluoro-3-iodobenzonitrile

6-Amino-2-fluoro-3-iodobenzonitrile has several applications across different fields:

  • Chemistry: It serves as an intermediate in the synthesis of complex organic molecules and heterocycles.
  • Biology: It is used in developing bioactive compounds and molecular probes.
  • Medicine: The compound acts as a precursor for synthesizing pharmaceutical agents with potential therapeutic effects.
  • Industry: It finds use in producing specialty chemicals and materials.

Interaction Studies of 6-Amino-2-fluoro-3-iodobenzonitrile

The interaction studies of 6-Amino-2-fluoro-3-iodobenzonitrile focus on its binding capacity with biological targets. These studies aim to elucidate the mechanisms by which this compound may exert its biological effects, particularly in drug discovery contexts. Understanding these interactions is crucial for optimizing its efficacy as a pharmaceutical agent.

Biological Activity of 6-Amino-2-fluoro-3-iodobenzonitrile

Research indicates that 6-Amino-2-fluoro-3-iodobenzonitrile may exhibit biological activity through its interactions with various molecular targets. The compound's structural features can enhance binding affinity and specificity towards enzymes, receptors, or nucleic acids. This makes it a candidate for further investigation in drug development, particularly in the synthesis of bioactive compounds with potential anticancer and antimicrobial properties.