3-Fluoro-4-iodobenzaldehyde
CAS No.:
1003709-57-6
M. Wt:
250.009
M. Fa:
C7H4FIO
InChI Key:
CGQJITDLUBMLFF-UHFFFAOYSA-N
Appearance:
Light brown solid
Names and Identifiers of 3-Fluoro-4-iodobenzaldehyde
CAS Number |
1003709-57-6 |
|---|---|
MDL Number |
MFCD07782055 |
IUPAC Name |
3-fluoro-4-iodobenzaldehyde |
InChI |
InChI=1S/C7H4FIO/c8-6-3-5(4-10)1-2-7(6)9/h1-4H |
InChIKey |
CGQJITDLUBMLFF-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC(=C(C=C1C=O)F)I |
UNSPSC Code |
12352100 |
Physical and chemical properties of 3-Fluoro-4-iodobenzaldehyde
Boiling Point |
264.5±25.0 °C at 760 mmHg |
|---|---|
Density |
2.0±0.1 g/cm3 |
Exact Mass |
249.929077 |
Flash Point |
113.8±23.2 °C |
Index of Refraction |
1.640 |
LogP |
3.00 |
Molecular Formula |
C7H4FIO |
Molecular Weight |
250.009 |
PSA |
17.07000 |
Storage condition |
under inert gas (nitrogen or Argon) at 2–8 °C |
Vapour Pressure |
0.0±0.5 mmHg at 25°C |
Safety Information of 3-Fluoro-4-iodobenzaldehyde
Applications of 3-Fluoro-4-iodobenzaldehyde
3-Fluoro-4-iodobenzaldehyde serves as a versatile intermediate in organic synthesis. Its applications include:
- Pharmaceuticals: Used in the synthesis of biologically active compounds and pharmaceuticals.
- Material Science: Acts as a building block for developing new materials with unique properties.
- Dyes and Pigments: Utilized in synthesizing dyes due to its ability to form stable colored complexes.
Interaction Studies of 3-Fluoro-4-iodobenzaldehyde
Interaction studies involving 3-fluoro-4-iodobenzaldehyde focus on its reactivity with various nucleophiles and electrophiles. These interactions are crucial for understanding its role in synthetic pathways and potential biological activity. The compound's reactivity profile may also provide insights into designing new derivatives with enhanced properties.
Physical sample testing spectrum (NMR) of 3-Fluoro-4-iodobenzaldehyde
