trans-Methyl 4-aminocyclohexanecarboxylate

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Reagent Code: #208993
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CAS Number 62456-15-9

science Other reagents with same CAS 62456-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.21 g/mol
Formula C₈H₁₅NO₂
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MDL Number MFCD12913678
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and analgesics. Its rigid cyclohexane backbone with defined stereochemistry makes it valuable for designing drugs with high selectivity and improved metabolic stability. Commonly employed in the preparation of receptor agonists and antagonists, especially those targeting GPCRs involved in pain modulation. Also utilized in medicinal chemistry for structure-activity relationship studies due to its ability to lock functional groups in specific spatial orientations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,360.00
inventory 1g
10-20 days ฿2,320.00
inventory 5g
10-20 days ฿7,910.00

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trans-Methyl 4-aminocyclohexanecarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and analgesics. Its rigid cyclohexane backbone with defined stereochemistry makes it valuable for designing drugs with high selectivity and improved metabolic stability. Commonly employed in the preparation of receptor agonists and antagonists, especially those targeting GPCRs involved in pain modulation. Also utilized in medicinal chemistry for structure-activity relationship

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and analgesics. Its rigid cyclohexane backbone with defined stereochemistry makes it valuable for designing drugs with high selectivity and improved metabolic stability. Commonly employed in the preparation of receptor agonists and antagonists, especially those targeting GPCRs involved in pain modulation. Also utilized in medicinal chemistry for structure-activity relationship studies due to its ability to lock functional groups in specific spatial orientations.

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