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19883-57-9

19883-57-9 structure
19883-57-9 structure

Name (2S)-2-amino-2-(4-fluorophenyl)acetic acid
Synonyms (S)-α-Amino-4-fluorobenzeneacetic acid
4-(4-Fluorophenyl)butyric acid
Benzeneacetic acid, .alpha.-amino-4-fluoro-, (.alpha.S)
(S)-4-Fluorophenylglycine //BP
Benzeneacetic acid, a-amino-4-fluoro-, (aS)
(2S)-2-amino-2-(4-fluorophenyl)aceticaci
(2S)-Amino(4-fluorophenyl)acetic acid
(S)-4-FLUOROPHENYLGLYCINE, (E.E.)
H-Phg(4-F)-OH
(S)-4-Fluorophenylgl
(S)-4-Fluorophenylglycine ee
(S)-2-amino-2-(4-fluorophenyl)acetic acid
(S)-4-FLUOROPHENYLGLYCINE HYDROCHLORIDE
4-FLUORO-L-ALPHA-PHENYLGLYCINE
MFCD00213799
4-Fluoro-L-2-phenylglycine>
4-fluoro-l-phenylglycine
(S)-4-FLUOROPHENYLGLYCINE-HCl
4-Fluorophenylglycine ee
inhibit,Inhibitor
(S)-(+)-4-(FLUOROPHENYL)GLYCINE
QVYZR DF &&S Form
(S)-4-Fluorophenylglycine, ( ee)
(alphaS)-alpha-Amino-4-fluorophenyl-acetic acid
2,5-Furandione,dihydro-6-phenyl
4-Fluoro-L-2-phenylglycine
L-AMINO-(4-FLUORO-PHENYL)-ACETIC ACID
(S)-4-Fluorophenyl gycine
4-Fluoro-L-α-phenylglycine
L-4-F-Phg-OH
Benzeneacetic acid, α-amino-4-fluoro-, (αS)
(S)-4-FLUOROPHENYLGLYCINE
(S)-AMINO-(4-FLUORO-PHENYL)-ACETIC ACID
(2S)-amino(4-fluorophenyl)ethanoic acid
(2S)-2-azaniumyl-2-(4-fluorophenyl)acetate
4-Fluoro-L-A-Phenylglycine
(S)-4-FL
(2S)-Amino(4-fluorophenyl)ethanoic acid
(S)-2-(4-Fluorophenyl)glycine
4-FLUORO-L-PHENYLGLYCINE
(S)-4-Fluorophenylglycine L-(4-Fluorophenyl) glycine
(S)-4-Fluorophenylglycine( ee)
L-4-Fluorophenylglycine
L-(P-FLUOROPHENYL)GLYCINE
4-Fluoro-L-alpha-phenylglycine
(S)-2-Amino-2-(4-fluorophenyl)acetic acid
4-Fluoro-L-2-phenylglycine/L-(4-Fluorophenyl)glycine
(S)-AMINO-(4-FLUORO-PHENYL)-ACETIC ACID HYDROCHLORIDE
4-Fluorophenylglycine, ee
p-fluorophenyl glycine
4-Fluoro-L-|á-phenylglycine
L-(4-FLUOROPHENYL) GLYCINE
Description (S)-2-Amino-2-(4-fluorophenyl)acetic acid is a Glycine (HY-Y0966) derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Density 1.3±0.1 g/cm3
Boiling Point 289.9±30.0 °C at 760 mmHg
Melting Point 300ºC
Molecular Formula C8H8FNO2
Molecular Weight 169.153
Flash Point 129.1±24.6 °C
Exact Mass 169.053909
PSA 63.32000
LogP 0.99
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.565
Hazard Codes Xi
Safety Phrases S24/25
WGK Germany 3
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