25616-02-8

Basic information

• Product Name: Boc-His(1-Boc)-OSu
• Synonyms: Boc-His(1-Boc)-OSu;Boc-His(tau-Boc)-OSu;Boc-His(t-Boc)-OSu;Nα,Nim-Bis-Boc-L-histidine N-hydroxysuccinimide ester;Boc-L-His(Boc)-OSu;Nα,Nim-Bis-Boc-L-histidineN-hydroxysuccinimide ester≥ 98% (Elemental analysis)
• CAS NO: 25616-02-8
• Molecular Formula: C₂₀H₂₈N₄O₈
• Molecular Weight: 452.461
• Mol File: 25616-02-8.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Store at 0°C
• Solubility: DMSO (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: Boc-His(1-Boc)-OSu(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-His(1-Boc)-OSu(25616-02-8)
• EPA Substance Registry System: Boc-His(1-Boc)-OSu(25616-02-8)

Safety Data

• Hazardous Substances Data: 25616-02-8(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 20866-46-0 N,1'-bis[(1,1-dimethylethoxy)carbonyl]-L-histidine 

Downstream Products

• 143117-79-7 [(S)-1-((1S,2S,4S)-4-Butylcarbamoyl-1-cyclohexylmethyl-2-hydroxy-5-methyl-hexylcarbamoyl)-2-(1H-imidazol-4-yl)-ethyl]-carbamic acid tert-butyl ester 
• 140661-03-6 (2S,3S,5S)-N-<1-cyclohexyl-3-hydroxyl-6-methyl-5-<<<2-(4-morpholinyl)ethoxy>carbonyl>amino>heptan-2-yl>(tert-butyloxycarbonyl)L-histidinamide 
• 105852-62-8 (2S,4S,5S)-5-[(S)-2-Amino-3-(1H-imidazol-4-yl)-propionylamino]-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid butylamide 
• 140661-00-3 {(S)-1-[(S)-1-((1S,2S,4S)-4-Butylcarbamoyl-1-cyclohexylmethyl-2-hydroxy-5-methyl-hexylcarbamoyl)-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester 

Relevant articles and documents

The First Dimeric Derivatives of the Glycopeptide Antibiotic Teicoplanin

Various dimeric derivatives of the glycopeptide antibiotic teicoplanin were prepared with the aim of increasing the activity of the parent compound against glycopeptide-resistant bacteria, primarily vancomycin-resistant enterococci. Starting from teicoplanin, four covalent dimers were prepared in two orientations, using an α,ω-bis-isothiocyanate linker. Formation of a dimeric cobalt coordination complex of an N-terminal L-histidyl derivative of teicoplanin pseudoaglycone has been detected and its antibacterial activity evaluated. The Co(III)-induced dimerization of the histidyl derivative was demonstrated by DOSY experiments. Both the covalent and the complex dimeric derivatives showed high activity against VanA teicoplanin-resistant enterococci, but their activity against other tested bacterial strains did not exceed that of the monomeric compounds.

Molecular recognition of a tris(histidine) ligand

Design and synthesis of a tri-Hg2+ complex to selectivity recognize a tris(histidine) ligand is presented.