1-(2-Methylfuran-3-yl)methanamine

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Reagent Code: #213539
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CAS Number 35801-15-1

science Other reagents with same CAS 35801-15-1

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scatter_plot Molecular Information
Weight 111.14 g/mol
Formula C₆H₉NO
badge Registry Numbers
MDL Number MFCD08435914
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting neurological and inflammatory conditions. Its furan ring structure with an amine side chain makes it valuable in medicinal chemistry for building more complex molecules with enhanced metabolic stability and receptor selectivity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to interact with biological targets in pests and weeds. Its reactivity allows for easy functionalization, enabling its use in combinatorial chemistry and high-throughput screening libraries.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,450.00

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1-(2-Methylfuran-3-yl)methanamine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting neurological and inflammatory conditions. Its furan ring structure with an amine side chain makes it valuable in medicinal chemistry for building more complex molecules with enhanced metabolic stability and receptor selectivity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to interact with biological

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting neurological and inflammatory conditions. Its furan ring structure with an amine side chain makes it valuable in medicinal chemistry for building more complex molecules with enhanced metabolic stability and receptor selectivity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to interact with biological targets in pests and weeds. Its reactivity allows for easy functionalization, enabling its use in combinatorial chemistry and high-throughput screening libraries.

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