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129460-09-9

129460-09-9 structure
129460-09-9 structure

Name (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoic acid
Synonyms FMOC-ASPTIC ACID-OTBU
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(1,1-dimethylethyl) ester
L-Fmoc-Asparticacid alpha-tert-butyl ester
4-tert-Butyl hydrogen N-((9H-fluoren-9-ylmethoxy)carbonyl)-L-aspartate
N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-L-ASPTIC ACID T-BUTYL ESTER
(3S)-4-(tert-butoxy)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid
Fmoc-L-aspartic acid 1-tert-butyl ester
FMOC-L-ASP-OTBU
Fmoc-Asp-OBu
L-Fmoc-Asptic acid alpha-tert-butyl ester
(2S)-4-tert-Butoxy-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid (non-preferred name)
Fmoc-L-asptic acid 1-tert-butyl ester
N-Fmoc-L-asptic Acid 1-tert-Butyl Ester
(9H-Fluoren-9-yl)MethOxy]carbonyl Asp-OtBu
N-Α-FMOC-L-ASPTIC ACID Β-T-BUTYL ESTER
1-tert-Butyl N-Fmoc-L-asptate
1-tert-ButylN-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asptate>
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asptic Acid 1-tert-Butyl Ester
(S)-2-(9H-FLUOREN-9-YLMETHOXYCBONYLAMINO)-SUCCINIC ACID 1-TERT-BUTYL ESTER
Fmoc-l-asptate-1-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
fmoc-asp-obut
N-ALPHA-L-ASPTIC ACID ALPHA TERT-BUTYL ESTER
4-(tert-butoxy)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid
L-Asptic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-(1,1-dimethylethyl) ester
N-Fmoc-L-asptic Ac
L-Fmoc-asptic acid α-t-butyl ester
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asptic Acid 1-tert-Butyl Ester 1-tert-Butyl N-Fmoc-L-asptate N-Fmoc-L-asptic Acid 1-tert-Butyl Ester Fmoc-Asp(OH)-OtBu
(R)-2-(9H-FLUOREN-9-YLMETHOXYCBONYLAMINO)-SUCCINIC ACID 1-TERT-BUTYL ESTER
L-Fmoc-Asptic acid α-tert-butyl ester
(S)-3-((((9H-Fluoren-9-yl)Methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid
N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-ASPTIC ACID ALPHA-T-BUTYL ESTER
FMOC-ASP-OTBU
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid
NALPHA-9-Fluorenylmethoxycbonyl-L-asptic acid ALPHA-tert-butyl ester
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-[(2-methyl-2-propanyl)oxy]-4-oxobutanoic acid
1-tert-Butyl N-Fmoc-L-aspartate
1-tert-Butyl N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-L-asptate , (LC&T
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asptic acid 1-(1,1-dimethylethyl ester
Fmoc-Asp-OtBu Novabiochem
FMOC-ASP-OTBU ( L isomer )
L-Fmoc-Aspartic acid α-tert-butyl ester
AmbotzFAA1356
N-ALPHA-(9-FLUORENYLMETHYLOXYCBONYL)-L-ASPTIC ACID ALPHA T-BUTYL ESTER
MFCD00065631
Fmoc-L-asptic acid-α-tert-butylester
N-ALPHA-FMOC-L-ASPTIC ACID ALPHA-T-BUTYL ESTER
(3S)-4-tert-Butoxy-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid (non-preferred name)
Fmoc-L-aspartic acid tert-butyl ester
N-α-FMOC-L-aspartic acid β-tert-butyl ester
Fmoc-Asp(tBu)-OH
Fmoc-Asp(OtBu)-OH
1-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asptate
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic Acid 1-tert-Butyl Ester
4-I-Phe
N-Fmoc-L-asptic acid α-tert-butyl ester
L-FMOC-ASPTIC ACID ALPHA-T-BUTYL ESTER
Fmoc-L-asptic acid-α-tert-butylester (HPLC)
Fmoc-asptic acidα-t-butyl ester
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asptic Acid 1-tert-Butyl Ester 1
fmoc-asp-otbu
(3S)-3-(9H-fluoren-9-ylmethoxycbonylamino)-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoic acid
L-Fmoc-Asptic acid alpha-tert-butyl ester //BP
Fmoc-Asp(OH)-OtBu
FMOC-L-ASPTIC ACID-ALPHA-T-BUTYL ESTER
moc-L-asptic acid 1-tert-butyl ester
(3S)-3-(9H-fluoren-9-ylmethoxycbonylamino)-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoicaci
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
FMOC-ASP-OBUT
L-Fmoc-Asptic acid α-|tert|-butyl ester
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

[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 1.3±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.
Hazard Codes Xi
Safety Phrases S24/25
HS Code 2924299090

~99%

129460-09-9 structure

129460-09-9

Literature: Tennant-Eyles, Richard J.; Fairbanks, Antony J. Tetrahedron Asymmetry, 1999 , vol. 10, # 2 p. 391 - 401

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129460-09-9 structure

129460-09-9

Literature: Journal of the Chemical Society. Perkin Transactions 1, , # 8 p. 1042 - 1049

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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%
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