Methyl trans-4-aminocyclohexanecarboxylate hydrochloride

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Reagent Code: #206912
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CAS Number 61367-07-5

science Other reagents with same CAS 61367-07-5

blur_circular Chemical Specifications

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Weight 193.67 g/mol
Formula C₈H₁₆ClNO₂
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MDL Number MFCD08274538
inventory_2 Storage & Handling
Storage Room temperature

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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 structure provides a rigid cyclohexane backbone with functional groups suitable for modifying potency and selectivity in drug candidates. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as metabolic stability and bioavailability. Also utilized in the preparation of enzyme inhibitors and receptor modulators due to its favorable stereochemistry and ability to mimic peptide-like structures.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿4,900.00
inventory 100g
10-20 days ฿18,930.00

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Methyl trans-4-aminocyclohexanecarboxylate hydrochloride
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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 structure provides a rigid cyclohexane backbone with functional groups suitable for modifying potency and selectivity in drug candidates. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as metabolic stability and bioavailability. Also utilized in the preparation of enzyme inhibitors and receptor modulators due to its f

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and analgesics. Its structure provides a rigid cyclohexane backbone with functional groups suitable for modifying potency and selectivity in drug candidates. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as metabolic stability and bioavailability. Also utilized in the preparation of enzyme inhibitors and receptor modulators due to its favorable stereochemistry and ability to mimic peptide-like structures.

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