(2R,6S)-4-(tert-Butoxycarbonyl)-6-methylmorpholine-2-carboxylic acid

98%

Reagent Code: #228695
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CAS Number 1346410-78-3

science Other reagents with same CAS 1346410-78-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.27 g/mol
Formula C₁₁H₁₉NO₅
badge Registry Numbers
MDL Number MFCD32670749
thermostat Physical Properties
Boiling Point 373.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.179±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules requiring stereochemical control. Its protected functional groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where the morpholine scaffold enhances solubility and metabolic stability. The Boc-protected amine and carboxylic acid handle enable peptide-like couplings and ring-forming reactions, making it valuable in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿29,820.00
inventory 100mg
10-20 days ฿38,430.00

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(2R,6S)-4-(tert-Butoxycarbonyl)-6-methylmorpholine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules requiring stereochemical control. Its protected functional groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where the morpholine scaffold enhances solubility and metabolic stability. The Boc-protected amine and carboxylic acid handle enable peptide-like coupling

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules requiring stereochemical control. Its protected functional groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where the morpholine scaffold enhances solubility and metabolic stability. The Boc-protected amine and carboxylic acid handle enable peptide-like couplings and ring-forming reactions, making it valuable in medicinal chemistry and drug discovery.

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