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73724-43-3

73724-43-3 structure
73724-43-3 structure

Name (2R)-3-(tert-butyldisulfanyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid
Synonyms Fmoc-Cys(S-t-Bu)-OH
Fmoc-Cys(tButhio)-OH
MFCD00042617
Nalpha-Fmoc-S-tert-butylthio-L-cysteine
EINECS 277-574-6
N-Fmoc-S-tert-butylthiol-L-cysteine
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butyldisulfanyl)propanoic acid
L-Alanine, 3-[(1,1-dimethylethyl)dithio]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Fmoc-L-Cys(StBu)-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-[(2-methyl-2-propanyl)disulfanyl]-L-alanine
Fmoc-Cys(StBu)-OH
Description N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(tert-butylthio)-L-cysteine 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 623.0±55.0 °C at 760 mmHg
Melting Point 73-77ºC
Molecular Formula C22H25NO4S2
Molecular Weight 431.568
Flash Point 330.6±31.5 °C
Exact Mass 431.122498
PSA 126.23000
LogP 6.95
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.621
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Risk Phrases 22-24/25
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3

~99%

73724-43-3 structure

73724-43-3

Literature: Gormer, Kristina; Waldmann, Herbert; Triola, Gemma Journal of Organic Chemistry, 2010 , vol. 75, # 5 p. 1811 - 1813

~81%

73724-43-3 structure

73724-43-3

Literature: Atherton, Eric; Pinori, Masimo; Sheppard, Robert C. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985 , p. 2057 - 2064
Precursor  4

DownStream  0