Fmoc-Asp-OAll structure
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Common Name | Fmoc-Asp-OAll | ||
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CAS Number | 144120-53-6 | Molecular Weight | 395.405 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 638.5±55.0 °C at 760 mmHg | |
Molecular Formula | C22H21NO6 | Melting Point | -95ºC (dec.) | |
MSDS | USA | Flash Point | 340.0±31.5 °C |
Use of Fmoc-Asp-OAll(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-4-oxobutanoic acid is an aspartic acid derivative[1]. |
Name | N-α-Fmoc-L-aspartic acid α-allyl ester |
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Synonym | More Synonyms |
Description | (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-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 | 1.3±0.1 g/cm3 |
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Boiling Point | 638.5±55.0 °C at 760 mmHg |
Melting Point | -95ºC (dec.) |
Molecular Formula | C22H21NO6 |
Molecular Weight | 395.405 |
Flash Point | 340.0±31.5 °C |
Exact Mass | 395.136902 |
PSA | 101.93000 |
LogP | 4.75 |
Vapour Pressure | 0.0±2.0 mmHg at 25°C |
Index of Refraction | 1.592 |
Storage condition | 2-8°C |
~96% Fmoc-Asp-OAll CAS#:144120-53-6 |
Literature: Ge, Jingyan; Li, Lin; Yao, Shao Q. Chemical Communications, 2011 , vol. 47, # 39 p. 10939 - 10941 |
~88% Fmoc-Asp-OAll CAS#:144120-53-6 |
Literature: Nuijens, Timo; Cusan, Claudia; Kruijtzer, John A. W.; Rijkers, Dirk T. S.; Liskamp, Rob M. J.; Quaedflieg, Peter J. L. M. Synthesis, 2009 , # 5 p. 809 - 814 |
~% Fmoc-Asp-OAll CAS#:144120-53-6 |
Literature: Tetrahedron Letters, , vol. 34, # 10 p. 1549 - 1552 |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
(S)-3-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-(allyloxy)-4-oxobutanoic acid |
EINECS 276-252-2 |
FMOC-L-ASP-OALL |
Fmoc-L-Asp(OAll)-OH |
FMOC-ASP-ALLYL ESTER |
Fmoc-L-Asp(OH)OAll |
FMOC-ASP-OAI |
Fmoc-Asp-Oal |
MFCD00467715 |
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(2-propen-1-yl) ester |
Fmoc-L-aspartic acid 1-allyl ester |
(2S)-4-(Allyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid |
Fmoc-L-Aspartic acid alpha-allyl ester |
Fmoc-Asp-OAll |
L-Fmoc-Asp-OAll |
N-[(9H-Fluoren-9-ylmethyloxycarbonyl)]-L-aspartic Acid 1-Allyl Ester |
N-Fmoc-L-aspartic Acid 1-Allyl Ester |
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-4-oxobutanoic acid |
1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate |
1-Allyl N-Fmoc-L-aspartate |
FMOC-ASPARTIC ACID-ALLYL ESTER |