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34582-32-6

34582-32-6 structure
34582-32-6 structure

Name (3S)-4-[(2-methylpropan-2-yl)oxy]-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid
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].
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

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Density 1.1±0.1 g/cm3
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
RIDADR NONH for all modes of transport

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34582-32-6 structure

34582-32-6

Literature: Ramalingam, Kondareddiar; Woodard, Ronald W. Journal of Organic Chemistry, 1988 , vol. 53, # 9 p. 1900 - 1903

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34582-32-6 structure

34582-32-6

Literature: Tetrahedron Letters, , vol. 44, # 28 p. 5251 - 5253

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34582-32-6 structure

34582-32-6

Literature: Journal of the Chemical Society - Perkin Transactions 1, , # 8 p. 855 - 866

~99%

34582-32-6 structure

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 ;

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34582-32-6 structure

34582-32-6

Literature: Tetrahedron, , vol. 57, # 30 p. 6557 - 6566

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34582-32-6 structure

34582-32-6

Literature: Journal of Organic Chemistry, , vol. 58, # 9 p. 2369 - 2376