(R)-Ethyl morpholine-2-carboxylate hydrochloride

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Reagent Code: #231273
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CAS Number 1820569-61-6

science Other reagents with same CAS 1820569-61-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.64 g/mol
Formula C₇H₁₄ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure supports the formation of peptidomimetics and other nitrogen-containing heterocycles. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure drugs. Also utilized in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system and metabolic disorder therapies. Serves as an intermediate in the manufacture of antiviral and anticancer agents. The hydrochloride salt form enhances stability and solubility in aqueous reaction media, facilitating downstream processing in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿600.00
inventory 250mg
10-20 days ฿1,250.00
inventory 1g
10-20 days ฿4,840.00
inventory 5g
10-20 days ฿18,330.00

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(R)-Ethyl morpholine-2-carboxylate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure supports the formation of peptidomimetics and other nitrogen-containing heterocycles. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure drugs. Also utilized in the preparation of enzyme inhibitors

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure supports the formation of peptidomimetics and other nitrogen-containing heterocycles. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure drugs. Also utilized in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system and metabolic disorder therapies. Serves as an intermediate in the manufacture of antiviral and anticancer agents. The hydrochloride salt form enhances stability and solubility in aqueous reaction media, facilitating downstream processing in multi-step syntheses.

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