2,5-Dibromo-6-fluorotoluene
Names and Identifiers of 2,5-Dibromo-6-fluorotoluene
CAS Number |
1000576-44-2 |
|---|---|
MDL Number |
MFCD09800767 |
IUPAC Name |
1,4-dibromo-2-fluoro-3-methylbenzene |
InChI |
InChI=1S/C7H5Br2F/c1-4-5(8)2-3-6(9)7(4)10/h2-3H,1H3 |
InChIKey |
DIHFJZRFCAKXCU-UHFFFAOYSA-N |
Canonical SMILES |
CC1=C(C=CC(=C1F)Br)Br |
UNSPSC Code |
12352100 |
Physical and chemical properties of 2,5-Dibromo-6-fluorotoluene
Boiling Point |
236.1±35.0 °C at 760 mmHg |
|---|---|
Density |
1.9±0.1 g/cm3 |
Exact Mass |
265.874176 |
Flash Point |
96.6±25.9 °C |
Index of Refraction |
1.567 |
LogP |
4.20 |
Molecular Formula |
C7H5Br2F |
Molecular Weight |
267.921 |
Storage condition |
Sealed in dry,Room Temperature |
Vapour Pressure |
0.1±0.5 mmHg at 25°C |
Safety Information of 2,5-Dibromo-6-fluorotoluene
Applications of 2,5-Dibromo-6-fluorotoluene
2,5-Dibromo-6-fluorotoluene finds applications across various fields:
- Organic Synthesis: It serves as an important intermediate in synthesizing more complex organic compounds.
- Material Science: The compound is explored for developing advanced materials, including polymers and pharmaceuticals.
- Biological Research: Its derivatives are utilized in studies related to protein interactions and imaging techniques due to their fluorescent nature.
Interaction Studies of 2,5-Dibromo-6-fluorotoluene
The interactions of 2,5-dibromo-6-fluorotoluene are primarily chemical rather than biological. The compound's reactivity can be influenced by environmental factors such as temperature, pH, and the presence of other chemicals. Understanding these interactions is crucial for optimizing its use in synthetic methodologies and industrial applications.
Biological Activity of 2,5-Dibromo-6-fluorotoluene
While primarily used as a synthetic intermediate, derivatives of 2,5-dibromo-6-fluorotoluene have been explored for biological applications. These derivatives serve as probes in biochemical research to study protein-protein interactions and other cellular processes due to their fluorescent properties. This makes them useful in imaging techniques and diagnostic applications.
Physical sample testing spectrum (NMR) of 2,5-Dibromo-6-fluorotoluene
