(R)-4-(tert-Butoxycarbonyl)morpholine-2-carboxylic acid

95%

Reagent Code: #230096
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CAS Number 884512-77-0

science Other reagents with same CAS 884512-77-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.25 g/mol
Formula C₁₀H₁₇NO₅
thermostat Physical Properties
Boiling Point 369.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites. Also utilized in asymmetric synthesis to introduce the morpholine ring with defined stereochemistry, enhancing metabolic stability and solubility in drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿410.00
250mg
10-20 days ฿710.00
1g
10-20 days ฿980.00
5g
10-20 days ฿3,340.00
25g
10-20 days ฿15,470.00
100g
10-20 days ฿59,590.00
(R)-4-(tert-Butoxycarbonyl)morpholine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites. Also utilized in asymmetric synthesis to int

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected amine and carboxylic acid functionalities make it ideal for peptide coupling and heterocycle formation in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and kinase inhibitors due to its structural compatibility with enzyme binding sites. Also utilized in asymmetric synthesis to introduce the morpholine ring with defined stereochemistry, enhancing metabolic stability and solubility in drug candidates.

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