trans-4-(Benzyloxy)cyclohexanamine

98%

Reagent Code: #153749
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CAS Number 98454-39-8

science Other reagents with same CAS 98454-39-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.3 g/mol
Formula C₁₃H₁₉NO
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MDL Number MFCD14584855
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

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 the creation of selective receptor modulators, including those targeting serotonin and dopamine receptors. Commonly employed in the preparation of experimental compounds for neurological disorders such as depression, anxiety, and Parkinson’s disease. Also utilized in medicinal chemistry for building chiral scaffolds due to its stable cyclohexane ring and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,750.00
inventory 250mg
10-20 days ฿4,550.00
inventory 1g
10-20 days ฿14,670.00

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trans-4-(Benzyloxy)cyclohexanamine
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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 the creation of selective receptor modulators, including those targeting serotonin and dopamine receptors. Commonly employed in the preparation of experimental compounds for neurological disorders such as depression, anxiety, and Parkinson’s disease. Also utilized in medicinal chemistry for building chiral scaffolds due to its stable cyclohexane ri

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of selective receptor modulators, including those targeting serotonin and dopamine receptors. Commonly employed in the preparation of experimental compounds for neurological disorders such as depression, anxiety, and Parkinson’s disease. Also utilized in medicinal chemistry for building chiral scaffolds due to its stable cyclohexane ring and functional group compatibility.

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