3-METHYLBENZOFURAN-2-CARBONYL CHLORIDE

97%

Reagent Code: #209841
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CAS Number 2256-86-2

science Other reagents with same CAS 2256-86-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.61 g/mol
Formula C₁₀H₇ClO₂
badge Registry Numbers
MDL Number MFCD01940394
thermostat Physical Properties
Melting Point 72-77 °C (lit.)
Boiling Point 119-121 °C(Press: 4 Torr)
inventory_2 Storage & Handling
Density 1.305±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive acid chloride group allows it to form amide or ester derivatives, making it valuable in constructing bioactive molecules. Commonly employed in the development of fragrances and flavoring agents due to the aromatic character of the benzofuran core. Also utilized in the synthesis of functional materials, including liquid crystals and organic semiconductors, where substituted benzofurans contribute to electronic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,980.00
3-METHYLBENZOFURAN-2-CARBONYL CHLORIDE
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive acid chloride group allows it to form amide or ester derivatives, making it valuable in constructing bioactive molecules. Commonly employed in the development of fragrances and flavoring agents due to the aromatic character of the benzofuran core. Also utilized in the synthesis of functional materials, including liquid crystals and organic semiconductors, where substituted benz

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive acid chloride group allows it to form amide or ester derivatives, making it valuable in constructing bioactive molecules. Commonly employed in the development of fragrances and flavoring agents due to the aromatic character of the benzofuran core. Also utilized in the synthesis of functional materials, including liquid crystals and organic semiconductors, where substituted benzofurans contribute to electronic properties.

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