structure of 2,3-Difluoro-4-bromonitrobenzene

2,3-Difluoro-4-bromonitrobenzene

CAS No.: 1003708-24-4
M. Wt: 237.986
M. Fa: C6H2BrF2NO2
InChI Key: GXNBBNIEEJTQST-UHFFFAOYSA-N
Appearance: (Yellow brown solid

Names and Identifiers of 2,3-Difluoro-4-bromonitrobenzene

CAS Number

1003708-24-4

MDL Number

MFCD09839215

IUPAC Name

1-bromo-2,3-difluoro-4-nitrobenzene

InChI

InChI=1S/C6H2BrF2NO2/c7-3-1-2-4(10(11)12)6(9)5(3)8/h1-2H

InChIKey

GXNBBNIEEJTQST-UHFFFAOYSA-N

Canonical SMILES

C1=CC(=C(C(=C1[N+](=O)[O-])F)F)Br

UNSPSC Code

12352100

Physical and chemical properties of 2,3-Difluoro-4-bromonitrobenzene

Boiling Point

265.5±35.0 °C at 760 mmHg

Density

1.9±0.1 g/cm3

Exact Mass

236.923691

Flash Point

114.3±25.9 °C

Index of Refraction

1.556

LogP

2.06

Molecular Formula

C6H2BrF2NO2

Molecular Weight

237.986

PSA

45.82000

Storage condition

Sealed in dry,Room Temperature

Vapour Pressure

0.0±0.5 mmHg at 25°C

Safety Information of 2,3-Difluoro-4-bromonitrobenzene

Pictograms

Signal Word

 Warning

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

Applications of 2,3-Difluoro-4-bromonitrobenzene

2,3-Difluoro-4-bromonitrobenzene finds utility in various fields:

  • Organic Synthesis: It serves as a crucial building block for synthesizing more complex organic molecules, especially in the pharmaceutical industry where it is used to develop drug candidates.
  • Material Science: The compound is being explored for applications in materials science, particularly in developing new materials with unique properties such as enhanced conductivity or reactivity.
  • Nanotechnology: It is utilized in the functionalization of nanomaterials like carbon nanotubes and graphene, enhancing their properties for applications in electronics and biomedicine.

Interaction Studies of 2,3-Difluoro-4-bromonitrobenzene

Studies on 2,3-Difluoro-4-bromonitrobenzene include investigations into its interactions with enzymes and other biological targets. These studies aim to elucidate its mechanism of action and potential inhibitory effects on specific biological pathways. For example, it may act as a substrate or inhibitor in enzymatic assays, providing insights into enzyme specificity and function.

Physical sample testing spectrum (NMR) of 2,3-Difluoro-4-bromonitrobenzene

Physical sample testing spectrum (NMR) of 2,3-Difluoro-4-bromonitrobenzene