1-(2,3-Dihydro-7-benzofuranyl)ethanone

≥95%

Reagent Code: #120804
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CAS Number 170730-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.19 g/mol
Formula C₁₀H₁₀O₂
badge Registry Numbers
MDL Number MFCD11656624
thermostat Physical Properties
Boiling Point 294.989°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,188.00
inventory 1g
10-20 days ฿5,796.00
inventory 5g
10-20 days ฿20,250.00
inventory 250mg
10-20 days ฿2,322.00
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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