Name | (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-phenylmethoxybutanoic acid |
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Synonyms |
MFCD00198201
(3S)-4-(Benzyloxy)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid Fmoc-Asp-OBzl Fmoc-L-Aspartic acid a-benzyl ester Fmoc-L-Aspartic |A-benzyl ester 1-benzyl N-fluoren-9-ylmethoxycarbonyl-L-aspartate Fmoc-L-Asparticacid-1-benzylester benzyl N-(9-fluorenylmethoxycarbonyl)-L-aspartic acid Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-(phenylmethyl) ester |
Description | Fmoc-Asp-Obzl is an aspartic 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 | 683.7±55.0 °C at 760 mmHg |
Molecular Formula | C26H23NO6 |
Molecular Weight | 445.464 |
Flash Point | 367.3±31.5 °C |
Exact Mass | 445.152527 |
PSA | 101.93000 |
LogP | 5.78 |
Vapour Pressure | 0.0±2.2 mmHg at 25°C |
Index of Refraction | 1.620 |
Storage condition | 2-8°C |
~97% 86060-83-5 |
Literature: Thieme, Karena; Schnell, Ingo Journal of the American Chemical Society, 2003 , vol. 125, # 40 p. 12100 - 12101 |
~% 86060-83-5 |
Literature: Carbohydrate Research, , vol. 174, p. 279 - 290 |
~%
Detail
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Literature: Chemical communications (Cambridge, England), , # 19 p. 1908 - 1909 |
~% 86060-83-5 |
Literature: Carbohydrate Research, , vol. 174, p. 279 - 290 |
~65% 86060-83-5 |
Literature: Kisfaludy, Lajos; Schoen, Istvan Synthesis, 1983 , # 4 p. 325 - 327 |
Precursor 7 | |
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DownStream 0 |