Ethyl (1S,2S)-2-aminocyclohexane-1-carboxylate hydrochloride

95%

Reagent Code: #185176
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CAS Number 180979-18-4

science Other reagents with same CAS 180979-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.7 g/mol
Formula C₉H₁₈ClNO₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its amine and ester functionalities allow for versatile chemical modifications, making it valuable in medicinal chemistry for constructing complex cyclic structures. Commonly employed in the preparation of enzyme inhibitors and receptor ligands due to its rigid cyclohexane backbone and defined stereochemistry. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,380.00
inventory 1g
10-20 days ฿52,010.00
Ethyl (1S,2S)-2-aminocyclohexane-1-carboxylate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its amine and ester functionalities allow for versatile chemical modifications, making it valuable in medicinal chemistry for constructing complex cyclic structures. Commonly employed in the preparation of enzyme inhibitors and receptor ligands due to its rigid cyclohexane backbone and defined stereochemistry. Also utilized in asymmetric synthesis t

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its amine and ester functionalities allow for versatile chemical modifications, making it valuable in medicinal chemistry for constructing complex cyclic structures. Commonly employed in the preparation of enzyme inhibitors and receptor ligands due to its rigid cyclohexane backbone and defined stereochemistry. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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