Top Suppliers:I want be here


95753-55-2

95753-55-2 structure
95753-55-2 structure

Name N-Fmoc-4-Nitro-L-Phenylalanine
Synonyms (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-nitrophenyl)propanoic acid
MFCD00057810
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
Fmoc-Phe(4-NO2)-OH
Fmoc-4-nitro-L-phenylalanine
Fmoc-Phe(4-NO2)-OH H2O
Description Fmoc-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):1793-908.

Density 1.4±0.1 g/cm3
Boiling Point 692.3±55.0 °C at 760 mmHg
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
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi: Irritant;
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3

~84%

95753-55-2 structure

95753-55-2

Literature: Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), , # 10 p. 1723 - 1728

~84%

95753-55-2 structure

95753-55-2

Literature: Tetrahedron Letters, , vol. 40, # 36 p. 6557 - 6560
Precursor  3

DownStream  1