1-(Aminomethyl)cyclopentanamine dihydrochloride

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Reagent Code: #130470
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CAS Number 123194-04-7

science Other reagents with same CAS 123194-04-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.65 g/mol
Formula C₆H₁₅ClN₂
badge Registry Numbers
MDL Number MFCD16547503
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, especially in the development of central nervous system (CNS) agents. Its structure supports the creation of bioactive molecules due to the presence of two amine groups in a constrained cycloaliphatic framework, enhancing binding selectivity in drug-receptor interactions. Commonly employed in the preparation of analgesics and neuromodulatory compounds. Also utilized in the design of novel amine-containing derivatives for research in neuropharmacology. Its dihydrochloride salt form improves stability and solubility, making it suitable for use in aqueous reaction media and purification processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,550.00
inventory 250mg
10-20 days ฿21,100.00

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1-(Aminomethyl)cyclopentanamine dihydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, especially in the development of central nervous system (CNS) agents. Its structure supports the creation of bioactive molecules due to the presence of two amine groups in a constrained cycloaliphatic framework, enhancing binding selectivity in drug-receptor interactions. Commonly employed in the preparation of analgesics and neuromodulatory compounds. Also utilized in the design of novel amine-containing derivatives for research i

Used primarily as a key intermediate in the synthesis of pharmaceuticals, especially in the development of central nervous system (CNS) agents. Its structure supports the creation of bioactive molecules due to the presence of two amine groups in a constrained cycloaliphatic framework, enhancing binding selectivity in drug-receptor interactions. Commonly employed in the preparation of analgesics and neuromodulatory compounds. Also utilized in the design of novel amine-containing derivatives for research in neuropharmacology. Its dihydrochloride salt form improves stability and solubility, making it suitable for use in aqueous reaction media and purification processes.

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