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Enzymes for Research, Diagnostic and Industrial Use

(S)-3-(1-allyl-5-fluoro-1H-indol-3-yl)-2-aminopropanoic acid

Cat No.
CEGZ-6610
Description
This compound is a non-natural amino acid derivative featuring an N-allyl-5-fluoroindole side chain. It is used as a building block in medicinal-chemistry and peptide-synthesis programs.
Applications
Medicinal-chemistry intermediate; non-natural amino acid derivative for peptide and small-molecule synthesis.
Appearance
Solid
Product Overview
The material is supplied as a solid with predicted boiling point, density and acidity values. The free amino acid and N-allyl indole motifs provide reactive handles for further functionalization.
CAS_No
3067192-74-6
Storage
Store in a tightly closed container at room temperature, protected from moisture and light.
Molecular Formula
C14H15FN2O2
Boiling Point
447.286 ± 45.00 °C (predicted, 25 °C, 760 Torr)
Density
1.278 ± 0.14 g/cm³ (predicted, 25 °C, 760 Torr)
Grade
Research grade
Notes
Research-use reagent; handle under standard laboratory conditions.

For research and industrial use only. Not intended for personal medicinal use. Certain food-grade products are suitable for formulation development in food and related applications.

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For research and industrial use only. Not intended for personal medicinal use. Certain food-grade products are suitable for formulation development in food and related applications.

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