18671-00-6

Basic information

• Product Name: Boc-Lys(Z)-Phe-OMe
• Synonyms: Boc-Lys(Z)-Phe-OMe
• CAS NO: 18671-00-6
• Molecular Weight: 541.645
• Mol File: 18671-00-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Boc-Lys(Z)-Phe-OMe(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-Lys(Z)-Phe-OMe(18671-00-6)
• EPA Substance Registry System: Boc-Lys(Z)-Phe-OMe(18671-00-6)

Safety Data

• Hazardous Substances Data: 18671-00-6(Hazardous Substances Data)

Upstream product

• 2389-45-9 Boc-Lys(Z)-OH 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 34404-36-9 Boc-Lys(Z)-OSu 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 13033-84-6 D-phenylalanine methyl ester hydrochloride 
• 1155-64-2 N₆-[(benzyloxy)carbonyl]-L-lysine 
• 1070-19-5 N-(tert-butyloxycarbonyl) azide 

Downstream Products

• 58328-63-5 Lys(N-Cbz)-Phe-OMe 
• 111334-44-2 H-Lys(Z)-Phe-OMe*TFA 
• 786709-51-1 2-[6-tert-butoxycarbonylamino-2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-hexanoylamino]-3-phenyl-propionic acid methyl ester 
• 786709-39-5 Boc-V-(δ-Boc)K-F 
• 786709-50-0 (S)-2-[(S)-6-Benzyloxycarbonylamino-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-hexanoylamino]-3-phenyl-propionic acid methyl ester 
• 18532-13-3 Boc-Ala-Ala-Lys(Z)-Phe-OMe 
• 111334-45-3 Boc-Ala-Ala-Lys(Z)-Phe-NHNH₂ 
• 1532594-91-4 C₄₄H₄₅N₃O₆ 
• 1532594-94-7 C₅₀H₆₂N₈O₁₀ 

Relevant articles and documents

Synthesis and characterization of peptide-cationic steroid antibiotic conjugates

(Chemical Equation Presented) New cationic steroid antibiotics have been prepared by conjugating tripeptides to a triamino analogue of cholic acid. These compounds were synthesized on a solid phase in an indexed library that was screened for antibacterial

Stimuli-responsive supramolecular gelation in ferrocene-peptide conjugates

Teaching an old dog new tricks: Ferrocene-dipeptide conjugates capable of forming gels in response to various external signals including sound, thermal, redox, and mechanical stress are reported (see figure). Interesting examples of how ferrocene-peptide conjugates can be exploited for the construction of organometallic gelators are demonstrated.