N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine

Modify Date: 2024-02-03 23:38:59

N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine Structure
N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine structure
Common Name N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine
CAS Number 1202704-91-3 Molecular Weight 328.36100
Density N/A Boiling Point N/A
Molecular Formula C15H24N2O6 Melting Point N/A
MSDS Chinese USA Flash Point 163.4 °F
Symbol GHS07
GHS07
Signal Word Warning

 Use of N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine


N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine is a lysine derivative[1].

 Names

Name Boc-Lys(Poc)-OH
Synonym More Synonyms

  Biological Activity

Description N2-[(1,1-Dimethylethoxy)carbonyl]-N6-[(2-propynyloxy)carbonyl]-L-lysine is a lysine 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

Molecular Formula C15H24N2O6
Molecular Weight 328.36100
Exact Mass 328.16300
PSA 113.96000
LogP 2.27580

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H317
Precautionary Statements P280
Flash Point(F) 163.4 °F
Flash Point(C) 73 °C

 Articles2

More Articles
Genetic encoding and labeling of aliphatic azides and alkynes in recombinant proteins via a pyrrolysyl-tRNA Synthetase/tRNA(CUA) pair and click chemistry.

J. Am. Chem. Soc. 131 , 8720-8721, (2009)

We demonstrate that an orthogonal Methanosarcina barkeri MS pyrrolysyl-tRNA synthetase/tRNA(CUA) pair directs the efficient, site-specific incorporation of N6-[(2-propynyloxy)carbonyl]-L-lysine, conta...

Synthesis of threefold glycosylated proteins using click chemistry and genetically encoded unnatural amino acids.

ChemBioChem. 10 , 2858-2861, (2009)

 Synonyms

(S)-2-(tert-butoxycarbonylamino)-6-((prop-2-ynyloxy)carbonylamino)hexanoic acid