(R)-4-Benzyl-3-morpholinecarboxylic Acid

≥97%

Reagent Code: #57105
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CAS Number 929047-50-7

science Other reagents with same CAS 929047-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.25 g/mol
Formula C₁₂H₁₅NO₃
badge Registry Numbers
MDL Number MFCD06799464
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of pharmaceuticals. Its structure, featuring a morpholine ring and a benzyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure drugs, where the (R)-configuration plays a critical role in biological activity. Additionally, it serves as an intermediate in the production of compounds targeting neurological and cardiovascular disorders. Its application extends to asymmetric catalysis, where it aids in the creation of chiral centers in various organic reactions.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,825.00

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(R)-4-Benzyl-3-morpholinecarboxylic Acid
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of pharmaceuticals. Its structure, featuring a morpholine ring and a benzyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure drugs, where the (R)-configuration plays a critical role in biological activity. Additionally, it serves as an intermediate in the production of com

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the development of pharmaceuticals. Its structure, featuring a morpholine ring and a benzyl group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the synthesis of enantiomerically pure drugs, where the (R)-configuration plays a critical role in biological activity. Additionally, it serves as an intermediate in the production of compounds targeting neurological and cardiovascular disorders. Its application extends to asymmetric catalysis, where it aids in the creation of chiral centers in various organic reactions.

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