(2R)-4-Morpholinyl(phenyl)acetic acid

95%

Reagent Code: #36466
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CAS Number 1007877-79-3

science Other reagents with same CAS 1007877-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.2524 g/mol
Formula C₁₂H₁₅NO₃
badge Registry Numbers
MDL Number MFCD20925681
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

(2R)-4-Morpholinyl(phenyl)acetic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate or building block in the synthesis of various biologically active compounds. Its structure, featuring both morpholine and phenylacetic acid moieties, makes it valuable for designing molecules with potential therapeutic applications, particularly in the development of drugs targeting neurological disorders, inflammation, or metabolic diseases. Researchers often employ this compound in the preparation of chiral molecules, leveraging its stereochemistry to create enantiomerically pure substances. Additionally, it may be used in the study of enzyme inhibition or receptor modulation due to its ability to interact with biological targets. Its applications extend to organic synthesis, where it contributes to the development of novel chemical entities with potential pharmacological properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,700.00
inventory 250mg
10-20 days ฿31,500.00

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(2R)-4-Morpholinyl(phenyl)acetic acid
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(2R)-4-Morpholinyl(phenyl)acetic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate or building block in the synthesis of various biologically active compounds. Its structure, featuring both morpholine and phenylacetic acid moieties, makes it valuable for designing molecules with potential therapeutic applications, particularly in the development of drugs targeting neurological disorders, inflammation, or metabolic diseases. Researchers often employ this compound in the preparation of chiral molecules, leveraging its stereochemistry to create enantiomerically pure substances. Additionally, it may be used in the study of enzyme inhibition or receptor modulation due to its ability to interact with biological targets. Its applications extend to organic synthesis, where it contributes to the development of novel chemical entities with potential pharmacological properties.
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