structure of 2,4-Dibromo-3,5-dichloroaniline

2,4-Dibromo-3,5-dichloroaniline

CAS No.: 1000574-35-5
M. Wt: 319.809
M. Fa: C6H3Br2Cl2N
InChI Key: PVBANICCLVRNTM-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 2,4-Dibromo-3,5-dichloroaniline

CAS Number

1000574-35-5

MDL Number

MFCD09878197

IUPAC Name

2,4-dibromo-3,5-dichloroaniline

InChI

InChI=1S/C6H3Br2Cl2N/c7-4-2(9)1-3(11)5(8)6(4)10/h1H,11H2

InChIKey

PVBANICCLVRNTM-UHFFFAOYSA-N

Canonical SMILES

C1=C(C(=C(C(=C1Cl)Br)Cl)Br)N

UNSPSC Code

12352100

Physical and chemical properties of 2,4-Dibromo-3,5-dichloroaniline

Boiling Point

353.7±37.0 °C at 760 mmHg

Density

2.2±0.1 g/cm3

Exact Mass

316.800903

Flash Point

167.7±26.5 °C

Index of Refraction

1.676

LogP

4.70

Molecular Formula

C6H3Br2Cl2N

Molecular Weight

319.809

Vapour Pressure

0.0±0.8 mmHg at 25°C

Safety Information of 2,4-Dibromo-3,5-dichloroaniline

Pictograms

Signal Word

 Warning

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

Applications of 2,4-Dibromo-3,5-dichloroaniline

2,4-Dibromo-3,5-dichloroaniline has several applications across various fields:

  • Chemistry: It serves as an intermediate in synthesizing various organic compounds.
  • Biology: The compound is investigated for its biological activities, particularly in antimicrobial research.
  • Medicine: Ongoing studies explore its potential therapeutic uses.
  • Industry: It is utilized in producing dyes, pigments, and other industrial chemicals.

Interaction Studies of 2,4-Dibromo-3,5-dichloroaniline

Research into the interactions of 2,4-Dibromo-3,5-dichloroaniline focuses on its reactivity with biological molecules and other chemical species. The halogen substituents play a critical role in determining the compound's reactivity and potential applications in drug development and material science.

Biological Activity of 2,4-Dibromo-3,5-dichloroaniline

Research indicates that 2,4-Dibromo-3,5-dichloroaniline exhibits potential biological activities. It has been studied for its antimicrobial and antifungal properties, making it a candidate for further exploration in pharmaceutical applications. The specific mechanisms of action involve interactions with molecular targets influenced by its halogen substituents.