2,3-Dihydrofuran
98%
- Product Code: 169405
Alias:
2,3-dihydrofuran;dihydroxyfuran
CAS:
1191-99-7
| Molecular Weight: | 70.09 g./mol | Molecular Formula: | C₄H₆O |
|---|---|---|---|
| EC Number: | 214-747-7 | MDL Number: | MFCD00003205 |
| Melting Point: | Boiling Point: | 54-55 °C(lit.) | |
| Density: | 0.927 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C, flammable area |
Product Description:
Used as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for heterocyclic compounds due to its reactive dihydrofuran ring. Commonly employed in cycloaddition reactions, such as Diels-Alder, to construct complex cyclic structures. Also utilized in the synthesis of natural products and functionalized tetrahydrofuran derivatives, which are important in medicinal chemistry. Its ability to undergo ring-opening and functionalization makes it valuable in creating chiral molecules for drug development.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98-100% |
| Refractive Index (N20/D) | 1.423-1.425 |
| Specific Gravity (20°C/20°C) | 0.923-0.928 |
| Appearance | colorless liquid |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25ml | 10-20 days | ฿380.00 |
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| 100ml | 10-20 days | ฿1,200.00 |
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| 500ml | 10-20 days | ฿5,000.00 |
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| 2.5L | 10-20 days | ฿22,150.00 |
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2,3-Dihydrofuran
Used as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for heterocyclic compounds due to its reactive dihydrofuran ring. Commonly employed in cycloaddition reactions, such as Diels-Alder, to construct complex cyclic structures. Also utilized in the synthesis of natural products and functionalized tetrahydrofuran derivatives, which are important in medicinal chemistry. Its ability to undergo ring-opening and functionalization makes it valuable in creating chiral molecules for drug development.
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