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136083-57-3

136083-57-3 structure
136083-57-3 structure

Name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanedioic acid
Synonyms N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-aspartic acid
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic acid
N-Fmoc-L-aspartic acid
D-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-(9-fluorenylmethoxycarbonyl)-L-aspartic acid
Fmoc-D-aspartic acid
Fmoc-D-Asp-OH
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}succinic acid
N-Fmoc-D-aspartic Acid
Fmoc-aspartic acid
MFCD01318740
Description Fmoc-D-Asp-OH 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 1.4±0.1 g/cm3
Boiling Point 587.2±45.0 °C at 760 mmHg
Molecular Formula C19H17NO6
Molecular Weight 355.341
Flash Point 308.9±28.7 °C
Exact Mass 355.105591
PSA 112.93000
LogP 3.55
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.628
Storage condition Store at RT.

~91%

136083-57-3 structure

136083-57-3

Literature: Commissariat A L'Energie Atomique; Universite De Picardie Jules Verne Patent: US2007/142324 A1, 2007 ; Location in patent: Page/Page column 8 ;

~96%

136083-57-3 structure

136083-57-3

Literature: Mehta, Anita; Jaouhari, Rabih; Benson, Timothy J.; Douglas, Kenneth T. Tetrahedron Letters, 1992 , vol. 33, # 37 p. 5441 - 5444

~%

136083-57-3 structure

136083-57-3

Literature: Journal of Peptide Science, , vol. 16, # 3 p. 159 - 164

~35%

136083-57-3 structure

136083-57-3

Literature: Chinchilla, Rafael; Dodsworth, David; Najera, Carmen; Soriano, Jose Tetrahedron Letters, 2001 , vol. 42, # 43 p. 7579 - 7581

~75%

136083-57-3 structure

136083-57-3

Literature: Sakina; Kawazura; Morihara; Yajima Chemical and Pharmaceutical Bulletin, 1988 , vol. 36, # 10 p. 3915 - 3919

~%

136083-57-3 structure

136083-57-3

Literature: Journal of Photochemistry and Photobiology A: Chemistry, , vol. 241, p. 52 - 57

~%

136083-57-3 structure

136083-57-3

Literature: Journal of Photochemistry and Photobiology A: Chemistry, , vol. 241, p. 52 - 57

~84%

136083-57-3 structure

136083-57-3

Literature: Singh, Suneel P.; Michaelides, Alex; Merrill, A. Rod; Schwan, Adrian L. Journal of Organic Chemistry, 2011 , vol. 76, # 16 p. 6825 - 6831
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%