structure of 2,6-Dibromo-4-fluoro-3-methyl-phenylamine

2,6-Dibromo-4-fluoro-3-methyl-phenylamine

CAS No.: 1000576-72-6
M. Wt: 282.93600
M. Fa: C7H6Br2FN
InChI Key: AHLMGMWQLJMGMF-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 1000576-72-6

CAS Number

1000576-72-6

MDL Number

MFCD09800776

IUPAC Name

2,6-dibromo-4-fluoro-3-methylaniline

InChI

InChI=1S/C7H6Br2FN/c1-3-5(10)2-4(8)7(11)6(3)9/h2H,11H2,1H3

InChIKey

AHLMGMWQLJMGMF-UHFFFAOYSA-N

Canonical SMILES

CC1=C(F)C=C(Br)C(N)=C1Br

UNSPSC Code

12352100

Physical and chemical properties of 1000576-72-6

Exact Mass

280.88500

LogP

3.82250

Molecular Formula

C7H6Br2FN

Molecular Weight

282.93600

PSA

26.02000

Safety Information of 1000576-72-6

Pictograms

Signal Word

 Warning

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

Applications of 1000576-72-6

2,6-Dibromo-4-fluoro-3-methylaniline has potential applications in various fields:

  • Agrochemicals: It may serve as an intermediate in the synthesis of pesticides or herbicides.
  • Pharmaceuticals: The compound could be explored for its biological activity as a lead compound in drug development.
  • Dyes and Pigments: Its unique structure may allow it to be used in dye formulations.

Interaction Studies of 1000576-72-6

Interaction studies involving 2,6-dibromo-4-fluoro-3-methylaniline typically focus on its binding affinity with biological targets such as enzymes or receptors. These studies are crucial for understanding its potential therapeutic effects and toxicity profiles. Preliminary studies suggest that similar compounds exhibit varying degrees of interaction based on structural modifications, indicating that further research is necessary to elucidate specific interactions.

Biological Activity of 1000576-72-6

Research indicates that compounds similar to 2,6-dibromo-4-fluoro-3-methylaniline exhibit significant biological activities, including antimicrobial and antifungal properties. The presence of halogen substituents often enhances these activities by increasing lipophilicity and altering the electronic properties of the molecule, potentially improving its interaction with biological targets.