Name | (2R)-6-amino-2-(phenylmethoxycarbonylamino)hexanoic acid |
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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]. |
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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 |
Density | 1.206g/cm3 |
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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 |
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RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
~47% 70671-54-4 |
Literature: Advanced Synthesis and Catalysis, , vol. 345, # 6-7 p. 830 - 834 |
~% 70671-54-4 |
Literature: Organic Letters, , vol. 6, # 21 p. 3781 - 3784 |
Precursor 2 | |
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DownStream 2 | |