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Boc2NOH
Nombre químico: Di-tert-butyl hydroxyiminodicarbonate // Sinónimos: Tert-butyl N-[(tert-butoxy)carbonyl]-N-hydroxycarbamate, Bis-N-Boc-hydroxylamine, Di-Boc-hydroxylamine, N,N-bis-Boc-hydroxylamine, N,N-Di(Boc)hydroxylamine
- Nº Artículo:RL-3660
- Nº CAS:142654-29-3
- Fórmula:C10H19NO5
- Storage temperature:-20°C
- Masa molecular:233,26 g/mol
- Pureza:min. 98%
from 84,00 €
description
This reagent can be used to synthesize various protected hydroxylamine derivatives that can be used for bio-conjugation and other applications.
references
Rapid Synthesis of Alkoxyamine Hydrochloride Derivatives from Alkyl Bromide and N,N’-Di-tert-butoxycarbonylhydroxylamine [(Boc)2NOH]; P. S. Jayasekara, K. A. Jacobson; Synth. Commun. 2014; 44: 2344-2347. https://doi.org/10.1080/00397911.2014.895014.
In situ growth of a stoichiometric PEG-like conjugate at a protein’s N-terminus with significantly improved pharmacokinetics; W. Gao, W. Liu, J. A. Mackay, M. R. Zalutsky, E. J. Toone, A. Chilkoti; PNAS 2009; 106(36): 15231-15236. https://doi.org/10.1073/pnas.0904378106.
4-Alkyloxyimino Derivatives of Uridine-5’-trphosphate: Distal Modification of Potent Agonists as a Strategy for Molecular Probes of P2Y2, P2Y4, and P2Y6 Receptors; P. S. Jayasekara, M. O. Barrett, C. B. Ball, K. A. Brown, E. Hammes, R. Balasubramanian, T. K. Harden, K. A. Jacobson; J. Med. Chem. 2014; 57: 3874-3883. https://doi.org/10.1021/jm500367e.
Synthesis of Constrained Tetracyclic Peptides by Consecutive CEPS, CLIPS, and Oxime Ligation; D. E. Streefkerk, M. Schmidt, J. H. Ippel, T. M. Hackeng, T. Nuijens, P. Timmerman, and J. H. van Maarseveen; Org. Lett. 2019; 21(7): 2095-2100. https://doi.org/10.1021/acs.orglett.9b00378.
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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