Name | (3S)-4-[(2-methylpropan-2-yl)oxy]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid |
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Synonyms |
MFCD00038272
1-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate |A-tert-Butyl-N-Boc-L-aspartate FC1234 Boc-ASp-OtBu N-(tert-Butoxycarbonyl)-L-aspartic Acid 1-tert-Butyl Ester Boc-L-Aspartic acid 1-tert-butyl ester Boc-L-Asp-OtBu L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester (3S)-4-[(2-Methyl-2-propanyl)oxy]-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid ASP002 N-Boc-L-aspartic Acid 1-tert-Butyl Ester 1-tert-Butyl N-Boc-L-aspartate (3S)-4-tert-Butoxy-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name) |
Description | (S)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid 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 | 1.1±0.1 g/cm3 |
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Boiling Point | 429.0±40.0 °C at 760 mmHg |
Melting Point | 101-103?C |
Molecular Formula | C13H23NO6 |
Molecular Weight | 289.325 |
Flash Point | 213.3±27.3 °C |
Exact Mass | 289.152527 |
PSA | 101.93000 |
LogP | 2.72 |
Vapour Pressure | 0.0±2.2 mmHg at 25°C |
Index of Refraction | 1.470 |
Storage condition | -15°C |
Hazard Codes | Xi |
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RIDADR | NONH for all modes of transport |
~76% 34582-32-6 |
Literature: Ramalingam, Kondareddiar; Woodard, Ronald W. Journal of Organic Chemistry, 1988 , vol. 53, # 9 p. 1900 - 1903 |
~% 34582-32-6 |
Literature: Tetrahedron Letters, , vol. 44, # 28 p. 5251 - 5253 |
~% 34582-32-6 |
Literature: Journal of the Chemical Society - Perkin Transactions 1, , # 8 p. 855 - 866 |
~99% 34582-32-6 |
Literature: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA; KUNG, Hank, F.; THOMPSON, Craig, B.; QU, Wenchao; PLOESSL, Karl Patent: WO2011/20018 A1, 2011 ; Location in patent: Page/Page column 23 ; |
~% 34582-32-6 |
Literature: Tetrahedron, , vol. 57, # 30 p. 6557 - 6566 |
~% 34582-32-6 |
Literature: Journal of Organic Chemistry, , vol. 58, # 9 p. 2369 - 2376 |
Precursor 6 | |
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DownStream 4 | |