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86060-83-5

86060-83-5 structure
86060-83-5 structure

Name (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-phenylmethoxybutanoic acid
Synonyms MFCD00198201
(3S)-4-(Benzyloxy)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid
Fmoc-Asp-OBzl
Fmoc-L-Aspartic acid a-benzyl ester
Fmoc-L-Aspartic |A-benzyl ester
1-benzyl N-fluoren-9-ylmethoxycarbonyl-L-aspartate
Fmoc-L-Asparticacid-1-benzylester
benzyl N-(9-fluorenylmethoxycarbonyl)-L-aspartic acid
Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-(phenylmethyl) ester
Description Fmoc-Asp-Obzl 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 683.7±55.0 °C at 760 mmHg
Molecular Formula C26H23NO6
Molecular Weight 445.464
Flash Point 367.3±31.5 °C
Exact Mass 445.152527
PSA 101.93000
LogP 5.78
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.620
Storage condition 2-8°C
Hazard Codes Xi
Safety Phrases 24/25

~97%

86060-83-5 structure

86060-83-5

Literature: Thieme, Karena; Schnell, Ingo Journal of the American Chemical Society, 2003 , vol. 125, # 40 p. 12100 - 12101

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86060-83-5 structure

86060-83-5

Literature: Carbohydrate Research, , vol. 174, p. 279 - 290

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Detail
Literature: Chemical communications (Cambridge, England), , # 19 p. 1908 - 1909

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86060-83-5 structure

86060-83-5

Literature: Carbohydrate Research, , vol. 174, p. 279 - 290

~65%

86060-83-5 structure

86060-83-5

Literature: Kisfaludy, Lajos; Schoen, Istvan Synthesis, 1983 , # 4 p. 325 - 327