(S)-3-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID

95%

Reagent Code: #238021
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CAS Number 720662-28-2

science Other reagents with same CAS 720662-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.22 g/mol
Formula C₁₀H₁₃NO₃
badge Registry Numbers
MDL Number MFCD04113678
thermostat Physical Properties
Melting Point 208-210 °C
Boiling Point 360.5±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.206±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its chiral structure makes it valuable in creating enantiomerically pure drugs, especially those targeting neurological disorders. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are explored for anticonvulsant, anxiolytic, and analgesic properties. Also employed in medicinal chemistry research to design novel ligands for neurotransmitter receptors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,420.00
inventory 1g
10-20 days ฿23,650.00
(S)-3-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its chiral structure makes it valuable in creating enantiomerically pure drugs, especially those targeting neurological disorders. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are explored for anticonvulsant, anxiolytic, and analgesic properties. Also employed in medicinal chemistry research to design novel ligands for n

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its chiral structure makes it valuable in creating enantiomerically pure drugs, especially those targeting neurological disorders. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are explored for anticonvulsant, anxiolytic, and analgesic properties. Also employed in medicinal chemistry research to design novel ligands for neurotransmitter receptors.

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