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130304-80-2

130304-80-2 structure
130304-80-2 structure

Name (2S)-4-cyclohexyloxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoic acid
Synonyms (3S)-4-(Cyclohexyloxy)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid
(2S)-4-(Cyclohexyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid
Fmoc-Asp(OcHex)-OH
AmbotzFAA1705
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-cyclohexyl ester
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-cyclohexyl ester
Fmoc-L-aspartic acid 4-cyclohexyl ester
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(cyclohexyloxy)-4-oxobutanoic acid
MFCD00135420
Fmoc-Asp(OcHx)-OH
Description Fmoc-Asp(OcHex)-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 1.3±0.1 g/cm3
Boiling Point 664.4±55.0 °C at 760 mmHg
Molecular Formula C25H27NO6
Molecular Weight 437.485
Flash Point 355.6±31.5 °C
Exact Mass 437.183838
PSA 101.93000
LogP 5.99
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.617
Storage condition -15°C
Hazard Codes Xi