Boc-3-(4-Pyridyl)-L-alanine

Modify Date: 2024-01-13 09:59:30

Boc-3-(4-Pyridyl)-L-alanine Structure
Boc-3-(4-Pyridyl)-L-alanine structure
Common Name Boc-3-(4-Pyridyl)-L-alanine
CAS Number 37535-57-2 Molecular Weight 266.293
Density 1.2±0.1 g/cm3 Boiling Point 454.3±40.0 °C at 760 mmHg
Molecular Formula C13H18N2O4 Melting Point 224ºC
MSDS USA Flash Point 228.5±27.3 °C

 Use of Boc-3-(4-Pyridyl)-L-alanine


Boc-Ala(4-pyridyl)-OH is an alanine derivative[1].

 Names

Name Boc-3-(4-Pyridyl)-L-alanine
Synonym More Synonyms

 Boc-3-(4-Pyridyl)-L-alanine Biological Activity

Description Boc-Ala(4-pyridyl)-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):1793-1114.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 454.3±40.0 °C at 760 mmHg
Melting Point 224ºC
Molecular Formula C13H18N2O4
Molecular Weight 266.293
Flash Point 228.5±27.3 °C
Exact Mass 266.126648
PSA 88.52000
LogP 1.47
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.530
Storage condition 2-8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi: Irritant;
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933399090

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2933399090
Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

MFCD00672528
Boc-3-(4-pyridyl)-Ala-OH
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-(4-pyridinyl)propanoic acid
4-Pyridinepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)-
N-(tert-Butoxycarbonyl)-3-pyridin-4-yl-L-alanine
(S)-2-(tert-butoxycarbonyl)-3-(pyridin-4-yl)propanoic acid
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-(4-pyridinyl)-L-alanine
Boc-L-4-pyridylalanine
(S)-2-((tert-Butoxycarbonyl)amino)-3-(pyridin-4-yl)propanoic acid
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pyridin-4-ylpropanoic acid
Boc-4-Pal-OH
N-Boc-3-(4-pyridyl)-L-alanine
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