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120791-76-6

120791-76-6 structure
120791-76-6 structure

Name tert-butyl (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxybutanoate
Synonyms Nalpha-Fmoc-L-threonine tert-Butyl Ester
Fmoc-L-threonine tert-butyl ester
Nα-Fmoc-L-threonine tert-Butyl Ester
N-fluorenylmethoxycarbonyl-threonine-tert-butyl ester
Fmoc-Thr-OtBu
Fmoc-threonine tert-butyl ester
Nα-[(9H-Fluoren-9-ylMethoxy)carbonyl]-L-threonine tert-Butyl Ester
Fmoc-Thr-tBu
Description Fmoc-Thr-OBu-t is a threonine 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.

Melting Point 100 ℃
Molecular Formula C23H27NO5
Molecular Weight 397.46400
Exact Mass 397.18900
PSA 84.86000
LogP 4.00710
Storage condition Refrigerator

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120791-76-6 structure

120791-76-6

Literature: Journal of Organic Chemistry, , vol. 68, # 17 p. 6795 - 6798

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120791-76-6 structure

120791-76-6

Literature: Liebigs Annalen der Chemie, , p. 751 - 770

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120791-76-6 structure

120791-76-6

Literature: Liebigs Annalen der Chemie, , p. 751 - 770

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120791-76-6 structure

120791-76-6

Literature: Liebigs Annalen der Chemie, , p. 751 - 770

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120791-76-6 structure

120791-76-6

Literature: European Journal of Organic Chemistry, , # 20-21 p. 3685 - 3689

~94%

120791-76-6 structure

120791-76-6

Literature: Journal of Organic Chemistry, , vol. 68, # 17 p. 6795 - 6798

~77%

120791-76-6 structure

120791-76-6

Literature: Angewandte Chemie (International Edition in English), , vol. 36, # 6 p. 618 - 621