N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine

Modify Date: 2024-01-03 14:40:04

N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine Structure
N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine structure
Common Name N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine
CAS Number 54613-99-9 Molecular Weight 414.880
Density 1.2±0.1 g/cm3 Boiling Point 608.3±55.0 °C at 760 mmHg
Molecular Formula C19H27ClN2O6 Melting Point 70-73 °C
MSDS N/A Flash Point 321.7±31.5 °C

 Use of N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine


Boc-Lys(2-Cl-Z)-OH is a lysine derivative[1].

 Names

Name (2S)-6-[(2-chlorophenyl)methoxycarbonylamino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
Synonym More Synonyms

  Biological Activity

Description Boc-Lys(2-Cl-Z)-OH is a lysine 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):1793-1144.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 608.3±55.0 °C at 760 mmHg
Melting Point 70-73 °C
Molecular Formula C19H27ClN2O6
Molecular Weight 414.880
Flash Point 321.7±31.5 °C
Exact Mass 414.155762
PSA 113.96000
LogP 3.73
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.532
Storage condition 2-8°C

 Safety Information

Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S36
WGK Germany 3

 Synonyms

N-(tert-Butoxycarbonyl)-N-{[(2-chlorobenzyl)oxy]carbonyl}-L-lysine
MFCD00038386
L-Lysine, N-[[(2-chlorophenyl)methoxy]carbonyl]-N-[(1,1-dimethylethoxy)carbonyl]-
(2S)-6-({[(2-Chlorobenzyl)oxy]carbonyl}amino)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)hexanoic acid
L-Lysine, N6-(((2-chlorophenyl)methoxy)carbonyl)-N2-((1,1-dimethylethoxy)carbonyl)-
N-{[(2-Chlorobenzyl)oxy]carbonyl}-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-lysine
AmbotzBAA1102
N6-(((2-Chlorophenyl)methoxy)carbonyl)-N2-((1,1-dimethylethoxy)carbonyl)-L-lysine
Boc-Lys(2-Cl-Z)-OH
N-Boc-N'-(2-chlorobenzyloxycarbonyl)-L-lysine
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