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167015-11-4

167015-11-4 structure
167015-11-4 structure

Name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanylpropanoic acid
Synonyms (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanylpropanoic acid
AmbotzFAA1035
Fmoc-S-trityl-D-cysteine
MFCD00151922
N-(9-Fluorenyl methoxy carbonyl)-S-trityl-L-cysteine
N-Fmoc-S-trityl-D-cysteine
Na-Fmoc-Ng-trityl-L-glutamine
N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-S-(triphenylMethyl)-L-cysteine
Fmoc-Cys(Trt)-OH
Fmoc-D-Cys(Trt)-OH
Fmoc-S-Trityl-L-Cysteine
N-Fmoc-S-trityl-L-cysteine
Cysteine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-(triphenylmethyl)-
(2R)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(tritylsulfanyl)propanoic acid
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-tritylcysteine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-(triphenylmethyl)-D-cysteine
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tritylthio)propanoic acid
Description Fmoc-D-Cys(Trt)-OH is a cysteine 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):1793-807.

Density 1.3±0.1 g/cm3
Boiling Point 763.4±60.0 °C at 760 mmHg
Melting Point 174 °C
Molecular Formula C37H31NO4S
Molecular Weight 585.711
Flash Point 415.5±32.9 °C
Exact Mass 585.197388
PSA 100.93000
LogP 9.96
Vapour Pressure 0.0±2.7 mmHg at 25°C
Index of Refraction 1.656
Storage condition -15°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport