N-Methyltetrahydrofuran-3-amine hydrochloride

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Reagent Code: #217444
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CAS Number 917882-94-1

science Other reagents with same CAS 917882-94-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.6 g/mol
Formula C₅H₁₂ClNO
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MDL Number MFCD09952761
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring chiral amine structures. Its cyclic ether and amine functionality make it valuable in creating complex organic molecules with high selectivity. Commonly employed in drug discovery for central nervous system agents and antiviral compounds due to its favorable solubility and stability profile in reaction sequences. Also utilized in asymmetric synthesis where the hydrochloride salt form enhances handling and reactivity control.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,070.00
inventory 1g
10-20 days ฿14,500.00
N-Methyltetrahydrofuran-3-amine hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring chiral amine structures. Its cyclic ether and amine functionality make it valuable in creating complex organic molecules with high selectivity. Commonly employed in drug discovery for central nervous system agents and antiviral compounds due to its favorable solubility and stability profile in reaction sequences. Also utilized in asymmetric synthesis where the hydrochloride salt fo

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring chiral amine structures. Its cyclic ether and amine functionality make it valuable in creating complex organic molecules with high selectivity. Commonly employed in drug discovery for central nervous system agents and antiviral compounds due to its favorable solubility and stability profile in reaction sequences. Also utilized in asymmetric synthesis where the hydrochloride salt form enhances handling and reactivity control.

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