Boc-N'-(2-chloro-Cbz)-D-lysine

Names

[ Name ]:
Boc-N'-(2-chloro-Cbz)-D-lysine

[Synonym ]:
(2R)-6-[(2-chlorophenyl)methoxycarbonylamino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
MFCD00065585
Boc-L-Lys(2-Cl-Z)-OH
D-Lysine, N-[[(2-chlorophenyl)methoxy]carbonyl]-N-[(1,1-dimethylethoxy)carbonyl]-
N-{[(2-Chlorobenzyl)oxy]carbonyl}-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-D-lysine
N-(tert-Butoxycarbonyl)-N-{[(2-chlorobenzyl)oxy]carbonyl}-D-lysine
Boc-D-Lys(2-Cl-Z)-OH

Biological Activity

[Description]:

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

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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

[ 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 ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Related Compounds

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