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117872-75-0

117872-75-0 structure
117872-75-0 structure

Name (2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylmethoxybutanoic acid
Synonyms L-Threonine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(phenylmethyl)-
(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzyloxy)butanoic acid
O-Benzyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-threonine
Fmoc-O-benzyl-L-threonine
MFCD00077073
Fmoc-Thr(Bzl)-OH
Description Fmoc-Thr(Bzl)-OH 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.

Density 1.3±0.1 g/cm3
Boiling Point 643.7±55.0 °C at 760 mmHg
Molecular Formula C26H25NO5
Molecular Weight 431.480
Flash Point 343.1±31.5 °C
Exact Mass 431.173279
PSA 84.86000
LogP 6.35
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.612
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3

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117872-75-0 structure

117872-75-0

Literature: Journal of the Chemical Society - Perkin Transactions 1, , # 5 p. 621 - 624

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117872-75-0 structure

117872-75-0

Literature: Journal of the Chemical Society - Perkin Transactions 1, , # 5 p. 621 - 624
Precursor  3

DownStream  0