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

95%

Reagent Code: #38268
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CAS Number 52448-15-4

science Other reagents with same CAS 52448-15-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.67 g/mol
Formula C₁₁H₁₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD06797629
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in biochemical research as a specialized amino acid derivative. Its structure, featuring an indole ring with a chloro substitution, makes it valuable in studying enzyme interactions, particularly those involving tryptophan metabolism. It is often employed in the synthesis of peptide-based compounds for investigating receptor binding and signal transduction pathways. Additionally, it serves as a precursor in the development of potential therapeutic agents targeting neurological disorders, given its structural similarity to neurotransmitters. Its applications also extend to organic synthesis, where it acts as a building block for creating complex molecules with biological activity.

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Test Parameter Specification
Appearance Off-white powder
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,035.00
inventory 100mg
10-20 days ฿5,022.00
inventory 1g
10-20 days ฿20,079.00

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(S)-2-Amino-3-(5-chloro-1H-indol-3-yl)propanoic acid
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This compound is primarily utilized in biochemical research as a specialized amino acid derivative. Its structure, featuring an indole ring with a chloro substitution, makes it valuable in studying enzyme interactions, particularly those involving tryptophan metabolism. It is often employed in the synthesis of peptide-based compounds for investigating receptor binding and signal transduction pathways. Additionally, it serves as a precursor in the development of potential therapeutic agents targeting neurological disorders, given its structural similarity to neurotransmitters. Its applications also extend to organic synthesis, where it acts as a building block for creating complex molecules with biological activity.
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