(S)-2-Amino-N-benzyl-3-(1H-indol-3-yl)propanamide

98%

Reagent Code: #233501
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CAS Number 125009-81-6

science Other reagents with same CAS 125009-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.36 g/mol
Formula C₁₈H₁₉N₃O
thermostat Physical Properties
Boiling Point 600.3±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.230±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents targeting neurological disorders, particularly serotonin receptor modulators. Its structural similarity to tryptophan allows incorporation into peptide-based drugs, enhancing blood-brain barrier penetration. Commonly employed in research for developing antidepressants and anti-migraine compounds due to its chiral stability and bioavailability in central nervous system applications. Also utilized in asymmetric synthesis to produce enantiomerically pure biologically active molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,060.00
inventory 250mg
10-20 days ฿32,410.00

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(S)-2-Amino-N-benzyl-3-(1H-indol-3-yl)propanamide
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Used as a key intermediate in the synthesis of pharmaceutical agents targeting neurological disorders, particularly serotonin receptor modulators. Its structural similarity to tryptophan allows incorporation into peptide-based drugs, enhancing blood-brain barrier penetration. Commonly employed in research for developing antidepressants and anti-migraine compounds due to its chiral stability and bioavailability in central nervous system applications. Also utilized in asymmetric synthesis to produce enanti

Used as a key intermediate in the synthesis of pharmaceutical agents targeting neurological disorders, particularly serotonin receptor modulators. Its structural similarity to tryptophan allows incorporation into peptide-based drugs, enhancing blood-brain barrier penetration. Commonly employed in research for developing antidepressants and anti-migraine compounds due to its chiral stability and bioavailability in central nervous system applications. Also utilized in asymmetric synthesis to produce enantiomerically pure biologically active molecules.

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