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70671-54-4

70671-54-4 structure
70671-54-4 structure

Name (2R)-6-amino-2-(phenylmethoxycarbonylamino)hexanoic acid
Synonyms Nalpha-Carbobenzoxy-D-lysine
Cbz-D-Lysine
N2-Cbz-D-lysine
Z-D-LYSINE
(2R)-6-Ammonio-2-{[(benzyloxy)carbonyl]amino}hexanoate
Z-D-Lys-OH
D-Norleucine, 6-ammonio-N-[(phenylmethoxy)carbonyl]-, inner salt
N-[(Benzyloxy)carbonyl]-D-lysine
Nalpha-Cbz-D-lysine
D-lysine, N-[(phenylmethoxy)carbonyl]-
N|A-Z-D-Lysine
N|A-Cbz-D-lysine
Nalpha-Z-D-Lysine
MFCD00067713
Description Z-D-Lys-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.

Density 1.206g/cm3
Boiling Point 497.0±45.0 °C at 760 mmHg
Melting Point 218ºC
Molecular Formula C14H20N2O4
Molecular Weight 280.320
Flash Point 254.4±28.7 °C
Exact Mass 280.142303
PSA 101.65000
LogP 1.36
Vapour Pressure 0.0±1.3 mmHg at 25°C
Index of Refraction 1.55
Storage condition Store at RT.
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3

~47%

70671-54-4 structure

70671-54-4

Literature: Advanced Synthesis and Catalysis, , vol. 345, # 6-7 p. 830 - 834

~%

70671-54-4 structure

70671-54-4

Literature: Organic Letters, , vol. 6, # 21 p. 3781 - 3784
Precursor  2

DownStream  2