1-(2,3-Dihydro-7-benzofuranyl)ethanone
≥95%
- Product Code: 120804
CAS:
170730-06-0
| Molecular Weight: | 162.19 g./mol | Molecular Formula: | C₁₀H₁₀O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11656624 | |
| Melting Point: | Boiling Point: | 294.989°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
1-(2,3-Dihydro-7-benzofuranyl)ethanone finds its primary application in organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a benzofuran ring, makes it a valuable building block for creating compounds with potential biological activity. It is often utilized in the development of drugs targeting neurological disorders, as the benzofuran moiety can interact with specific receptors in the brain. Additionally, this compound is employed in the synthesis of fragrances and flavoring agents, contributing to the creation of complex aromatic profiles. Its versatility in chemical reactions, such as alkylation and acylation, further enhances its utility in industrial and research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,188.00 |
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| 0.250 | 10-20 days | ฿2,322.00 |
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| 1.000 | 10-20 days | ฿5,796.00 |
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| 5.000 | 10-20 days | ฿20,250.00 |
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1-(2,3-Dihydro-7-benzofuranyl)ethanone
1-(2,3-Dihydro-7-benzofuranyl)ethanone finds its primary application in organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a benzofuran ring, makes it a valuable building block for creating compounds with potential biological activity. It is often utilized in the development of drugs targeting neurological disorders, as the benzofuran moiety can interact with specific receptors in the brain. Additionally, this compound is employed in the synthesis of fragrances and flavoring agents, contributing to the creation of complex aromatic profiles. Its versatility in chemical reactions, such as alkylation and acylation, further enhances its utility in industrial and research settings.
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