N-Boc-L-lysine-d4

Chemical Name:N-Boc-L-lysine-d4
Synonyms:Boc-Lys-OH-d4; N2-[(1,1-Dimethylethoxy)carbonyl]- L-lysine-d4; N2-Carboxy-L-lysine N2-tert-Butyl Ester-d4; (S)-6-Amino-2-(tert-butoxycarbonylamino)hexanoic Acid-d4; N-α-(tert-Butoxycarbonyl)-L-lysine-d4; N2-tert-Butoxycarbonyl-L-lysine-d4; NSC 343721-d4; Nα-BOC-L-lysine-d4; α-N-tert-Butoxycarbonyl-L-lysine-d4; α-tert-Butoxycarbonyl-L-lysine-d4;
Alternate CAS #:13734-28-6
Molecular Formula:C₁₁H₁₈D₄N₂O₄
Molecular Weight:250.33
Category:Building Blocks; Chiral Molecules; Nucleic Acid; Isotopic Labeled Analogues; Pharmaceutical/API Drug Impurities/Metabolites;
Applications:N-Boc-L-lysine-d4 is the deuterated form of N-Boc-L-lysine (B656900), which is a protected analogue of a major amino acid participating in the binding of AcH to proteins. N-Boc-L-lysine as well as other t-butoxycarbonyl (Boc) amino acids can be converted to their respective amino acids via cleavage of the urethane bond.
References:Tuma, D.J. et al.: Alc. Clin. Exp. Res., 11, 579 (1987); Ohshiro, T. et al.: Appl. Microbiol. Biotechnol., 48, 546 (1997);
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