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16881-33-7

16881-33-7 structure
16881-33-7 structure
  • Name: Z-Tyr-OtBu.H2O
  • Chemical Name: z-tyr-otbu h2o
  • CAS Number: 16881-33-7
  • Molecular Formula: C21H25NO5
  • Molecular Weight: 371.427
  • Catalog: Research Areas Others
  • Create Date: 2018-07-25 15:19:35
  • Modify Date: 2024-01-09 06:01:18
  • Z-Tyr-OtBu is a tyrosine derivative[1].

Name z-tyr-otbu h2o
Synonyms N-(benzyloxycarbonyl)-L-tyrosine tert-butyl ester
Cbz-Tyr-O-t-Bu
Z-L-tyrosinetertutylestermonohydrate
Z-L-TYROSINE T-BUTYL ESTER HYDRATE
L-Tyrosine, N-[(phenylmethoxy)carbonyl]-, 1,1-dimethylethyl ester
(S)-N-(benzyloxycarbonyl)tyrosine tert-butyl ester
2-Methyl-2-propanyl N-[(benzyloxy)carbonyl]-L-tyrosinate
Z-L-Tyr-O-tBu
Cbz-L-tyrosine tert-butyl ester
N-benzyloxycarbonyl tyrosine tert-butyl ester
L-TYROSINE,N-[(PHENYLMETHOXY)CARBONYL]-,1,1-DIMETHYLETHYL ESTER
Z-Tyr-OtBu.H2O
Z-L-TYROSINE-T-BUTYL ESTER MONOHYDRATE
N-[(phenylmethoxy)carbonyl]-L-tyrosine 1,1-dimethylethyl ester
Z-Tyr-OtBu
(S)-tert-butyl 2-(benzyloxycarbonylamino)-3-(4-hydroxyphenyl)propanoate
Z-Tyr-OtBu·H2O
Description Z-Tyr-OtBu is a tyrosine 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 543.8±50.0 °C at 760 mmHg
Molecular Formula C21H25NO5
Molecular Weight 371.427
Flash Point 282.7±30.1 °C
Exact Mass 371.173279
PSA 84.86000
LogP 4.49
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.563

~95%

16881-33-7 structure

16881-33-7

Literature: Palmer, Francine N.; Lach, Franck; Poriel, Cyril; Pepper, Adrian G.; Bagley, Mark C.; Slawin, Alexandra M. Z.; Moody, Christopher J. Organic and Biomolecular Chemistry, 2005 , vol. 3, # 20 p. 3805 - 3811

~%

16881-33-7 structure

16881-33-7

Literature: Anderson,G.W.; Callahan,F.M. Journal of the American Chemical Society, 1960 , vol. 82, p. 3359 - 3363

~88%

16881-33-7 structure

16881-33-7

Literature: Chevallet, Pierre; Garrouste, Patrick; Malawska, Barbara; Martinez, Jean Tetrahedron Letters, 1993 , vol. 34, # 46 p. 7409 - 7412