(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID

(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID Structure
CAS No.
16626-02-1
Chemical Name:
(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID
Synonyms
H-L-Trp(5-F)-OH*H2O;L-5-FLUOROTRYPTOPHAN;5-FLUORO-L-TRYPTOPHAN;H-5-FLUORO-TRP-OH H2O;Tryptophan Impurity 54;5-fluoro-L-tryptophans;L-Tryptophan, 5-fluoro-;5-Fluoro-tryptophan monohydrate;L-5-fluorotryptophan monohydrate;5-FLUORO-L-TRYPTOPHAN MONOHYDRATE
CBNumber:
CB1274150
Molecular Formula:
C11H11FN2O2
Molecular Weight:
222.22
MOL File:
16626-02-1.mol
MSDS File:
SDS
Modify Date:
2022/12/30 16:20:48

(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID Properties

Melting point 238-239 °C
Boiling point 450.7±45.0 °C(Predicted)
Density 1.442±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 2.21±0.10(Predicted)
BRN 5052680

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Safety Statements  22-24/25
WGK Germany  3
10
HS Code  2933998090

(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 47568 5-Fluoro-L-tryptophan ≥98.0% (HPLC) 16626-02-1 25MG ₹8080 2022-06-14 Buy
Product number Packaging Price Buy
47568 25MG ₹8080 Buy

(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID Chemical Properties,Uses,Production

Uses

Exogenous 5-fluoro-Trp is incorporated into proteins in normal protein synthesis. Since 19F is a useful reporter group, this provides a method for studying enzyme mechanisms by NMR.

Biochem/physiol Actions

5-Fluoro-Trp is nonspecifically cytotoxic. It is believed this is due to malfunctioning enzymes that have had replacements of Trp residues by 5-fluoro-Trp. However, at least one case is known where 5-fluoro-Trp substitution leads to significantly greater catalytic activity.

Purification Methods

Recrystallise it from EtOH, aqueous EtOH or AcOH. Also purify it by passage through a Dowex AG1x2 (acetate form) column and recrystallise the L-enantiomer (from enzymic enrichment) from H2O/EtOH, m 158-163o(dec), [] D -8.3o (c 2.5, N NaOH). [Coy et al. Biochemistry 13 3550 1974, Beilstein 22/14 V 116.]

(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID Suppliers

Global( 78)Suppliers
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5-FLUORO-L-TRYPTOPHAN 5-FLUORO-L-TRYPTOPHAN MONOHYDRATE H-5-FLUORO-TRP-OH H2O L-5-FLUOROTRYPTOPHAN (S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID 5-Fluoro-tryptophan monohydrate H-L-Trp(5-F)-OH*H2O L-5-fluorotryptophan monohydrate (S)-5-Fluoro-α-amino-1H-indole-3-propionic acid (S)-α-Amino-5-fluoro-1H-indole-3-propionic acid (S)-2-AMino-3-(5-fluoro-1H-indol-3-yl)propanoic acid L-Tryptophan, 5-fluoro- (2S)-2-amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid 5-Fluoro-L-tryptophan >=98.0% (HPLC) Tryptophan Impurity 54 5-fluoro-L-tryptophans 16626-02-1 C11H11FN2O2H2O BioChemical Biochemicals and Reagents Enzyme Inhibitors Enzyme Inhibitors by Type Enzymes, Inhibitors, and Substrates Substrate Analogs Unnatural Amino Acid Derivatives Tryptophan Derivatives F Enzyme Inhibitors by Type Alphabetic Substrate AnalogsPeptide Synthesis FA - FLEnzyme Inhibitors Indoles and derivatives