(R)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid

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Reagent Code: #231456
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CAS Number 55325-48-9

science Other reagents with same CAS 55325-48-9

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Weight 238.67 g/mol
Formula C₁₁H₁₁ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used in biochemical and pharmaceutical research as a chiral building block for synthesizing serotonin receptor ligands and analogs. It serves as a key intermediate in the development of neuropharmacological agents targeting mood disorders, sleep regulation, and neurological diseases. Its structural similarity to tryptophan and serotonin makes it valuable in studying enzyme substrates and inhibitors involved in neurotransmitter metabolism. Also applied in asymmetric synthesis and peptide modification to enhance biological stability and receptor selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,450.00
inventory 250mg
10-20 days ฿8,870.00
inventory 1g
10-20 days ฿28,620.00

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(R)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid
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Used in biochemical and pharmaceutical research as a chiral building block for synthesizing serotonin receptor ligands and analogs. It serves as a key intermediate in the development of neuropharmacological agents targeting mood disorders, sleep regulation, and neurological diseases. Its structural similarity to tryptophan and serotonin makes it valuable in studying enzyme substrates and inhibitors involved in neurotransmitter metabolism. Also applied in asymmetric synthesis and peptide modification to enha
Used in biochemical and pharmaceutical research as a chiral building block for synthesizing serotonin receptor ligands and analogs. It serves as a key intermediate in the development of neuropharmacological agents targeting mood disorders, sleep regulation, and neurological diseases. Its structural similarity to tryptophan and serotonin makes it valuable in studying enzyme substrates and inhibitors involved in neurotransmitter metabolism. Also applied in asymmetric synthesis and peptide modification to enhance biological stability and receptor selectivity.
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