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58438-04-3

58438-04-3 structure
58438-04-3 structure

Name Boc-3-(2-Naphthyl)-L-alanine
Synonyms (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(2-naphthyl)propanoic acid (non-preferred name)
N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-L-alanine
MFCD00079671
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-naphthalen-2-ylpropanoic acid
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-(2-naphthyl)propanoic acid
N-(tert-butoxycarbonyl)-3-naphthalen-2-yl-L-alanine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-(2-naphthyl)-L-alanine
2-naphthalenepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)-
Boc-3-(2-Naphthyl)-Alanine
Description Boc-2-Nal-OH is an alanine 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):1793-1121.

Density 1.2±0.1 g/cm3
Boiling Point 512.2±43.0 °C at 760 mmHg
Melting Point 95ºC
Molecular Formula C18H21NO4
Molecular Weight 315.364
Flash Point 263.6±28.2 °C
Exact Mass 315.147064
PSA 75.63000
LogP 4.19
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.587
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3
Precursor  0

DownStream  1