Name | (2R)-2-amino-5-oxo-5-phenylmethoxypentanoic acid |
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Synonyms |
H-Glu(OBzl)-OH;; L-Glutamic acid γ-benzyl ester
L-Glutamic acid γ-benzyl ester L-Glutamic acid 5-benzyl ester MFCD00063111 Glutamic acid, 5-benzyl ester, L- γ-Benzyl L-glutamate L-Glutamic acid, 5-(phenylmethyl) ester H-Glu(OBzl)-OH Glutamic acid, 5-(phenylmethyl) ester 5-Benzyl L-GlutaMate (2S)-2-Amino-5-(benzyloxy)-5-oxopentanoic acid D-Glutamic Acid 5-Benzyl Ester L-Glutamic acid, 5- (phenylmethyl) ester H-D-Glu(OBzl)-OH gamma-Benzyl L-glutamate AmbotzHAA6230 5-Benzyl D-GlutaMate D-glutamic acid, 5-(phenylmethyl) ester (2R)-2-Amino-5-(benzyloxy)-5-oxopentanoic acid D-Glutamicacidγ-benzylester |
Description | H-D-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 | 1.2±0.1 g/cm3 |
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Boiling Point | 426.1±45.0 °C at 760 mmHg |
Melting Point | 176ºC |
Molecular Formula | C12H15NO4 |
Molecular Weight | 237.252 |
Flash Point | 211.5±28.7 °C |
Exact Mass | 237.100113 |
PSA | 89.62000 |
LogP | 1.56 |
Vapour Pressure | 0.0±1.1 mmHg at 25°C |
Index of Refraction | 1.555 |
Storage condition | Store at RT. |
Hazard Codes | Xi |
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~57% 2578-33-8 |
Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 10, # 12 p. 1361 - 1363 |
~% 2578-33-8 |
Literature: Tetrahedron, , vol. 2, p. 211,226 Acta Chimica Academiae Scientiarum Hungaricae, , vol. 6, p. 219,226 |
Precursor 3 | |
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DownStream 9 | |