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117106-20-4

117106-20-4 structure
117106-20-4 structure

Name Fmoc-Nalpha-methyl-O-t-butyl-L-threonine
Synonyms (2S,3R)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-[(2-methylpropan-2-yl)oxy]butanoic acid
Fmoc-N-Me-Thr(tBu)-OH
MFCD02094431
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-O-(2-methyl-2-propanyl)-L-threonine
Fmoc-N-methyl-O-tert-butyl-L-threonine
N-Fmoc-N-Methyl-O-tert-butyl-L-threonine
L-Threonine, O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-
O-tert-Butyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-threonine
(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(tert-butoxy)butanoic acid
Description Fmoc-N-Me-Thr(tBu)-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 1.2±0.1 g/cm3
Boiling Point 562.4±50.0 °C at 760 mmHg
Molecular Formula C24H29NO5
Molecular Weight 411.491
Flash Point 293.9±30.1 °C
Exact Mass 411.204559
PSA 76.07000
LogP 5.93
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.568
Storage condition -15°C
Hazard Codes Xi
RIDADR NONH for all modes of transport
HS Code 2922509090

~43%

117106-20-4 structure

117106-20-4

Literature: Galpin; Mohammed; Patel Tetrahedron, 1988 , vol. 44, # 6 p. 1773 - 1782
Precursor  2

DownStream  0

HS Code 2922509090
Summary 2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
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