Boc-Asp-OtBu structure
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Common Name | Boc-Asp-OtBu | ||
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CAS Number | 34582-32-6 | Molecular Weight | 289.325 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 429.0±40.0 °C at 760 mmHg | |
Molecular Formula | C13H23NO6 | Melting Point | 101-103?C | |
MSDS | Chinese USA | Flash Point | 213.3±27.3 °C |
Use of Boc-Asp-OtBu(S)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is an aspartic acid derivative[1]. |
Name | (3S)-4-[(2-methylpropan-2-yl)oxy]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid |
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Synonym | More Synonyms |
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% Boc-Asp-OtBu CAS#:34582-32-6 |
Literature: Ramalingam, Kondareddiar; Woodard, Ronald W. Journal of Organic Chemistry, 1988 , vol. 53, # 9 p. 1900 - 1903 |
~% Boc-Asp-OtBu CAS#:34582-32-6 |
Literature: Tetrahedron Letters, , vol. 44, # 28 p. 5251 - 5253 |
~% Boc-Asp-OtBu CAS#:34582-32-6 |
Literature: Journal of the Chemical Society - Perkin Transactions 1, , # 8 p. 855 - 866 |
~99% Boc-Asp-OtBu CAS#: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 ; |
~% Boc-Asp-OtBu CAS#:34582-32-6 |
Literature: Tetrahedron, , vol. 57, # 30 p. 6557 - 6566 |
~% Boc-Asp-OtBu CAS#:34582-32-6 |
Literature: Journal of Organic Chemistry, , vol. 58, # 9 p. 2369 - 2376 |
Precursor 6 | |
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DownStream 4 | |
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) |