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21947-98-8

21947-98-8 structure
21947-98-8 structure

Name (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-tritylsulfanylpropanoic acid
Synonyms L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-(triphenylmethyl)-
MFCD00038251
(R)-2-(tert-Butoxycarbonylamino)-3-(tritylthio)propanoic acid
N-[(1,1-dimethylethoxy)carbonyl]-S-trityl-L-cysteine
n-(tert-butoxycarbonyl)-s-trityl-l-cysteine
S-trityl-N-Boc-(R)-cysteine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-S-trityl-L-cysteine
N-t-butyloxycarbonyl-S-trityl-L-cysteine
S-trityl-N-Boc-cysteine
N-t-butoxycarbonyl-S-trityl-L-Cysteine
Boc-S-trityl-L-cysteine
Boc-Cys(Trt)-OH
EINECS 244-674-6
N-Boc-S-trityl-L-cysteine
Description (R)-2-((tert-Butoxycarbonyl)amino)-3-(tritylthio)propanoic acid 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 1.2±0.1 g/cm3
Boiling Point 610.9±55.0 °C at 760 mmHg
Melting Point 143-146 °C(lit.)
Molecular Formula C27H29NO4S
Molecular Weight 463.589
Flash Point 323.3±31.5 °C
Exact Mass 463.181732
PSA 100.93000
LogP 7.52
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.596
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3

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21947-98-8 structure

21947-98-8

Literature: Venkateswara Rao, Boddu; Dhokale, Snehal; Rajamohanan, Pattuparambil R.; Hotha, Srinivas Chemical Communications, 2013 , vol. 49, # 92 p. 10808 - 10810

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Literature: Organic Letters, , vol. 7, # 13 p. 2615 - 2618

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Literature: European Journal of Medicinal Chemistry, , vol. 50, p. 383 - 392

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21947-98-8 structure

21947-98-8

Literature: Chemische Berichte, , vol. 102, p. 1048 - 1052

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21947-98-8 structure

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Literature: Canadian Journal of Chemistry, , vol. 57, p. 1388 - 1396