Cis 4-aMinocyclohexanecarboxylic acid hydrochloride

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Reagent Code: #156747
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CAS Number 118785-97-0

science Other reagents with same CAS 118785-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.64456 g/mol
Formula C₇H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD14279363
thermostat Physical Properties
Melting Point 217 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of muscle relaxants and central nervous system agents. Its stereochemistry makes it valuable for creating biologically active compounds with high selectivity. Commonly employed in research settings to design analogs of gamma-aminobutyric acid (GABA) for studying neurological pathways and developing treatments for neurological disorders. Also utilized in the preparation of chiral building blocks for asymmetric synthesis in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,000.00
inventory 5g
10-20 days ฿8,000.00
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Cis 4-aMinocyclohexanecarboxylic acid hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of muscle relaxants and central nervous system agents. Its stereochemistry makes it valuable for creating biologically active compounds with high selectivity. Commonly employed in research settings to design analogs of gamma-aminobutyric acid (GABA) for studying neurological pathways and developing treatments for neurological disorders. Also utilized in the preparation of chiral building blocks for asymmetric

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of muscle relaxants and central nervous system agents. Its stereochemistry makes it valuable for creating biologically active compounds with high selectivity. Commonly employed in research settings to design analogs of gamma-aminobutyric acid (GABA) for studying neurological pathways and developing treatments for neurological disorders. Also utilized in the preparation of chiral building blocks for asymmetric synthesis in medicinal chemistry.

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