Boc-3-(2-Naphthyl)-L-alanine

Modify Date: 2024-01-02 22:23:06

Boc-3-(2-Naphthyl)-L-alanine Structure
Boc-3-(2-Naphthyl)-L-alanine structure
 Common Name Boc-3-(2-Naphthyl)-L-alanine
CAS Number 58438-04-3 Molecular Weight 315.364
Density 1.2±0.1 g/cm3 Boiling Point 512.2±43.0 °C at 760 mmHg
Molecular Formula C18H21NO4 Melting Point 95ºC
MSDS USA Flash Point 263.6±28.2 °C

 Use of Boc-3-(2-Naphthyl)-L-alanine


Boc-2-Nal-OH is an alanine derivative[1].

 Names

Name Boc-3-(2-Naphthyl)-L-alanine
Synonym More Synonyms

 Boc-3-(2-Naphthyl)-L-alanine Biological Activity

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.

 Chemical & Physical Properties

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

 Safety Information

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 & DownStream

Precursor  0

DownStream  1

 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
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