Z-Ile-Bt

Modify Date: 2024-01-14 11:52:39

Z-Ile-Bt Structure
Z-Ile-Bt structure
Common Name Z-Ile-Bt
CAS Number 1072442-07-9 Molecular Weight 366.414
Density 1.3±0.1 g/cm3 Boiling Point N/A
Molecular Formula C20H22N4O3 Melting Point N/A
MSDS USA Flash Point N/A

 Use of Z-Ile-Bt


Z-Ile-Bt is an isoleucine derivative[1].

 Names

Name Benzyl [(2S,3S)-1-(1H-benzotriazol-1-yl)-3-methyl-1-oxo-2-pentanyl]carbamate
Synonym More Synonyms

 Z-Ile-Bt Biological Activity

Description Z-Ile-Bt is an isoleucine 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.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Molecular Formula C20H22N4O3
Molecular Weight 366.414
Exact Mass 366.169189
LogP 4.29
Index of Refraction 1.620

 Safety Information

RIDADR NONH for all modes of transport

 Articles6

More Articles
Benzotriazole-mediated syntheses of depsipeptides and oligoesters.

J. Org. Chem. 76 , 4884-4893, (2011)

Reactions of O-Pg(α-hydroxyacyl)benzotriazoles with (a) unprotected α-hydroxycarboxylic acids, (b) amino acids, and (c) amines afforded, respectively, chirally pure (a) oligoesters, (b) depsidipeptide...

Efficient preparation of aminoxyacyl amides, aminoxy hybrid peptides, and alpha-aminoxy peptides.

J. Org. Chem. 74th ed.,, 8690-8694, (2009)

N-(Pg-alpha-aminoxy acids) 1a-g are converted to N-(Pg-alpha-aminoxyacyl)benzotriazoles 2a-g, which react under mild conditions with amines, alpha-amino acids/alpha-dipeptides, and alpha-aminoxy acids...

Abdelmajeid, A.; Tala, S. R.; Amine, M. S.; Katritzky, A. R.

Synthesis , 2995-3005, (2011)

 Synonyms

Carbamic acid, N-[(1S,2S)-1-(1H-1,2,3-benzotriazol-1-ylcarbonyl)-2-methylbutyl]-, phenylmethyl ester
Benzyl [(2S,3S)-1-(1H-benzotriazol-1-yl)-3-methyl-1-oxo-2-pentanyl]carbamate