N-Methyl-1-(3-methyloxetan-3-YL)methanamine

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Reagent Code: #220710
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CAS Number 915919-90-3

science Other reagents with same CAS 915919-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.17 g/mol
Formula C₆H₁₃NO
badge Registry Numbers
MDL Number MFCD08691435
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports blood-brain barrier penetration, making it valuable in designing neuroactive drugs. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as metabolic stability and solubility. Also utilized in the preparation of bioactive molecules where a constrained amine moiety is required. Its oxetane ring contributes to improved binding affinity and reduced lipophilicity in drug candidates.

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inventory 1g
10-20 days ฿17,260.00

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N-Methyl-1-(3-methyloxetan-3-YL)methanamine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports blood-brain barrier penetration, making it valuable in designing neuroactive drugs. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as metabolic stability and solubility. Also utilized in the preparation of bioactive molecules where a constrained amine moiety is required. Its oxetane ring contributes to impro

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports blood-brain barrier penetration, making it valuable in designing neuroactive drugs. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as metabolic stability and solubility. Also utilized in the preparation of bioactive molecules where a constrained amine moiety is required. Its oxetane ring contributes to improved binding affinity and reduced lipophilicity in drug candidates.

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