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177966-63-1

177966-63-1 structure
177966-63-1 structure

Name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-nitrophenyl)propanoic acid
Synonyms MFCD00237029
AmbotzFAA1685
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-nitrophenyl)propanoic acid
Fmoc-D-4-Nitrophe
Fmoc-D-phe(4-NO2)-OH
L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-nitro-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-D-phenylalanine
Fmoc-D-4-NO2-Phe-OH
D-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-nitro-
Fmoc-4-nitro-D-phenylalanine
Description Fmoc-D-Phe(4-NO2)-OH is a phenylalanine 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):1793-935.

Density 1.4±0.1 g/cm3
Boiling Point 692.3±55.0 °C at 760 mmHg
Melting Point 215-225ºC
Molecular Formula C24H20N2O6
Molecular Weight 432.425
Flash Point 372.5±31.5 °C
Exact Mass 432.132141
PSA 121.45000
LogP 5.14
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.650
Storage condition 2-8°C
Hazard Codes Xi: Irritant;
RIDADR NONH for all modes of transport