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174132-31-1

174132-31-1 structure
174132-31-1 structure

Name Fmoc-p(NH-Boc)-L-Phe-OH
Synonyms N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-L-phenylalanine
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)phenyl]propanoic acid
RARECHEM BK PT 0176
L-Phenylalanine, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-aminophenyl)propanoic acid
MFCD03094894
Fmoc-Phe(4-NHBoc)-OH
Description (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-((tert-butoxycarbonyl)amino)phenyl)propanoic acid 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):1793-952.

Density 1.3±0.1 g/cm3
Boiling Point 671.0±55.0 °C at 760 mmHg
Molecular Formula C29H30N2O6
Molecular Weight 502.558
Flash Point 359.6±31.5 °C
Exact Mass 502.210388
PSA 113.96000
LogP 6.18
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.622
Storage condition -15°C
Hazard Codes Xi