structure of 5-Bromo-3-chloro-2-iodotoluene

5-Bromo-3-chloro-2-iodotoluene

CAS No.: 1000573-87-4
M. Wt: 331.37600
M. Fa: C7H5BrClI
InChI Key: NUXOMLHLSLRWMX-UHFFFAOYSA-N

Names and Identifiers of 5-Bromo-3-chloro-2-iodotoluene

CAS Number

1000573-87-4

MDL Number

MFCD09878185

IUPAC Name

5-bromo-1-chloro-2-iodo-3-methylbenzene

InChI

InChI=1S/C7H5BrClI/c1-4-2-5(8)3-6(9)7(4)10/h2-3H,1H3

InChIKey

NUXOMLHLSLRWMX-UHFFFAOYSA-N

Canonical SMILES

CC1=CC(Br)=CC(Cl)=C1I

UNSPSC Code

12352100

Physical and chemical properties of 5-Bromo-3-chloro-2-iodotoluene

Boiling Point

301.8±37.0 °C(Predicted)

Density

2.125±0.06 g/cm3(Predicted)

Exact Mass

329.83100

LogP

4.01550

Molecular Formula

C7H5BrClI

Molecular Weight

331.37600

Safety Information of 5-Bromo-3-chloro-2-iodotoluene

Pictograms

Signal Word

 Warning

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

Applications of 5-Bromo-3-chloro-2-iodotoluene

5-Bromo-3-chloro-2-iodotoluene has several applications across different fields:

  • Chemical Research: Used as a reagent in organic synthesis for developing new compounds.
  • Pharmaceutical Development: Its reactivity makes it valuable in drug design and development processes.
  • Material Science: Employed in creating advanced materials through coupling reactions that form complex structures.

Interaction Studies of 5-Bromo-3-chloro-2-iodotoluene

Studies have shown that 5-Bromo-3-chloro-2-iodotoluene interacts with various biological systems. Its interactions with cytochrome P450 enzymes highlight its potential role in drug metabolism and toxicity studies. Additionally, its ability to form covalent bonds with biomolecules suggests that it could influence cellular signaling pathways and metabolic processes.