3,4-Dihydro-2H-pyran-2-carbaldehyde
CAS No.:
100-73-2
M. Wt:
112.127
M. Fa:
C6H8O2
InChI Key:
NPWYTMFWRRIFLK-UHFFFAOYSA-N
Appearance:
Liquid oil
Names and Identifiers of 3,4-Dihydro-2H-pyran-2-carbaldehyde
CAS Number |
100-73-2 |
|---|---|
EC Number |
202-884-5 |
IUPAC Name |
3,4-dihydro-2H-pyran-2-carbaldehyde |
InChI |
InChI=1S/C6H8O2/c7-5-6-3-1-2-4-8-6/h2,4-6H,1,3H2 |
InChIKey |
NPWYTMFWRRIFLK-UHFFFAOYSA-N |
Canonical SMILES |
C1CC(OC=C1)C=O |
UNII |
49SA3RBS5H |
UN Number |
2607 |
Physical and chemical properties of 3,4-Dihydro-2H-pyran-2-carbaldehyde
Boiling Point |
185.1±39.0 °C at 760 mmHg |
|---|---|
Density |
1.2±0.1 g/cm3 |
Exact Mass |
112.052429 |
Flash Point |
118 °F (NFPA, 2010) |
Index of Refraction |
1.547 |
LogP |
-0.17 |
Melting Point |
-100ºC |
Molecular Formula |
C6H8O2 |
Molecular Weight |
112.127 |
PSA |
26.30000 |
Vapour Pressure |
0.7±0.4 mmHg at 25°C |
Safety Information of 3,4-Dihydro-2H-pyran-2-carbaldehyde
Applications of 3,4-Dihydro-2H-pyran-2-carbaldehyde
3,4-Dihydro-2H-pyran-2-carbaldehyde has several notable applications:
- Organic Synthesis: It serves as an intermediate in the synthesis of more complex organic molecules.
- Pharmaceutical Development: Its derivatives are explored for their potential therapeutic effects, particularly in anti-inflammatory drugs.
Biological Activity of 3,4-Dihydro-2H-pyran-2-carbaldehyde
Research indicates that derivatives of 3,4-dihydro-2H-pyran-2-carbaldehyde exhibit biological activity, particularly as adenosine receptor agonists. These compounds have shown potential in mediating anti-inflammatory actions through their interaction with A2A and A3 adenosine receptors. Such activities suggest a role in pharmacological applications.
Physical sample testing spectrum (NMR) of 3,4-Dihydro-2H-pyran-2-carbaldehyde
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