![]() Fmoc-Asp-OtBu structure
|
Common Name | Fmoc-Asp-OtBu | ||
---|---|---|---|---|
CAS Number | 129460-09-9 | Molecular Weight | 411.448 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 617.4±55.0 °C at 760 mmHg | |
Molecular Formula | C23H25NO6 | Melting Point | N/A | |
MSDS | USA | Flash Point | 327.2±31.5 °C |
Use of Fmoc-Asp-OtBuFmoc-Asp-OtBu is an aspartic acid derivative[1]. |
Name | (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoic acid |
---|---|
Synonym | More Synonyms |
Description | Fmoc-Asp-OtBu 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 |
Density | 1.3±0.1 g/cm3 |
---|---|
Boiling Point | 617.4±55.0 °C at 760 mmHg |
Molecular Formula | C23H25NO6 |
Molecular Weight | 411.448 |
Flash Point | 327.2±31.5 °C |
Exact Mass | 411.168182 |
PSA | 101.93000 |
LogP | 5.16 |
Vapour Pressure | 0.0±1.9 mmHg at 25°C |
Index of Refraction | 1.576 |
Storage condition | Store at RT. |
~99% Fmoc-Asp-OtBu CAS#:129460-09-9 |
Literature: Tennant-Eyles, Richard J.; Fairbanks, Antony J. Tetrahedron Asymmetry, 1999 , vol. 10, # 2 p. 391 - 401 |
~% Fmoc-Asp-OtBu CAS#:129460-09-9 |
Literature: Journal of the Chemical Society. Perkin Transactions 1, , # 8 p. 1042 - 1049 |
~%
Detail
|
Literature: Synthesis, , # 7 p. 571 - 572 |
HS Code | 2924299090 |
---|---|
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% |
L-Fmoc-Aspartic acid α-tert-butyl ester |
(3S)-3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid |
1-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate |
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1,1-dimethylethyl) ester |
AmbotzFAA1356 |
fmoc-asp-otbu |
4-tert-Butyl hydrogen N-((9H-fluoren-9-ylmethoxy)carbonyl)-L-aspartate |
Fmoc-L-aspartic acid 1-tert-butyl ester |
MFCD00065631 |
(3S)-4-tert-Butoxy-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid (non-preferred name) |
Fmoc-L-aspartic acid tert-butyl ester |
fmoc-asp-obut |
N-α-FMOC-L-aspartic acid β-tert-butyl ester |
Fmoc-Asp(tBu)-OH |
Fmoc-Asp(OH)-OtBu |
(2S)-4-tert-Butoxy-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid (non-preferred name) |
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid |
N-Fmoc-L-aspartic acid 1-tert-butyl ester |
L-Fmoc-Asparticacidalpha-tert-butylester |
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester |
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid |
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic Acid 1-tert-Butyl Ester |
1-tert-Butyl N-Fmoc-L-aspartate |
L-Fmoc-Asparticacid alpha-tert-butyl ester |