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144120-54-7

144120-54-7 structure
144120-54-7 structure

Name (4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-prop-2-enoxypentanoic acid
Synonyms (S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(allyloxy)-5-oxopentanoic acid
MFCD00467718
Fmoc-Glu-OAll
Fmoc-L-glutamic acid |A-allyl ester
L-Fmoc-Glu-OAll
Fmoc-Glu-OAllyl
Fmoc-L-glutamic acid 1-allyl ester
Description Fmoc-Glu-OAll is a glutamic 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 1.264g/cm3
Boiling Point 652.3ºC at 760 mmHg
Melting Point 118-122ºC
Molecular Formula C23H23NO6
Molecular Weight 409.43200
Flash Point 348.3ºC
Exact Mass 409.15300
PSA 101.93000
LogP 3.87860
Vapour Pressure 6.64E-18mmHg at 25°C
Index of Refraction 1.585
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090

~88%

144120-54-7 structure

144120-54-7

Literature: Nuijens, Timo; Cusan, Claudia; Kruijtzer, John A. W.; Rijkers, Dirk T. S.; Liskamp, Rob M. J.; Quaedflieg, Peter J. L. M. Synthesis, 2009 , # 5 p. 809 - 814

~%

144120-54-7 structure

144120-54-7

Literature: Tetrahedron Letters, , vol. 34, # 10 p. 1549 - 1552
Precursor  3

DownStream  0

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%