Name | 5-Benzyl N-Carbobenzoxy-L-glutamate |
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Synonyms |
MFCD00065697
L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-, 5-(phenylmethyl) ester (2S)-5-(Benzyloxy)-2-{[(benzyloxy)carbonyl]amino}-5-oxopentanoic acid (2S)-5-oxo-5-phenylmethoxy-2-(phenylmethoxycarbonylamino)pentanoic acid Z-Glu(OBzl)-OH |
Description | Z-Glu(OBzl)-OH is a glutamic acid 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 | 1.3±0.1 g/cm3 |
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Boiling Point | 594.3±50.0 °C at 760 mmHg |
Melting Point | 76 °C |
Molecular Formula | C20H21NO6 |
Molecular Weight | 371.384 |
Flash Point | 313.2±30.1 °C |
Exact Mass | 371.136902 |
PSA | 101.93000 |
LogP | 3.95 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.575 |
Storage condition | Store at RT. |
~90% 5680-86-4 |
Literature: Desjardins, Michel; Garneau, Sylvie; Desgagnes, Julie; Lacoste, Lucille; Yang, Fu; Lapointe, Jacques; Chenevert, Robert Bioorganic Chemistry, 1998 , vol. 26, # 1 p. 1 - 13 |
~% 5680-86-4 |
Literature: Journal of the Chemical Society, , p. 3239,3243 |
~% 5680-86-4 |
Literature: Chemische Berichte, , vol. 66, p. 1288,1290 |
~% 5680-86-4 |
Literature: Journal of the Chemical Society, , p. 3239,3243 |
~% 5680-86-4 |
Literature: Chemische Berichte, , vol. 95, p. 7 - 16 Chemische Berichte, , vol. 96, p. 204 - 212 |