20866-46-0
20866-46-0
Chemical Structure
Boc-His(Boc)-OH
Synonym(s): N,N'-Di-tert-butoxycarbonyl-L-histidine
- CAS No.: 20866-46-0
- Formula:C16H25N3O6
- Molecular Weight:355.39
IUPAC Name: Na,Nt-bis(tert-butoxycarbonyl)-L-histidine
InChIKey: IXHPIPUIOSSAIS-NSHDSACASA-N
SMILES: O=C(O)[C@H](CC1=CN(C(OC(C)(C)C)=O)C=N1)NC(OC(C)(C)C)=O
Biological Activity: Boc-His (Boc)-OH (N,N'-Di-tert-butoxycarbonyl-L-histidine) is a protected L-histidine derivative carrying N,N'-di-tert-butoxycarbonyl protecting groups, and also serves as a peptide synthesis building block[1][2].
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Boc-His(Boc)-OH | 95.0% | Boc-His (Boc)-OH (N,N'-Di-tert-butoxycarbonyl-L-histidine) is a protected L-histidine derivative carrying N,N'-di-tert-butoxycarbonyl protecting groups, and also serves as a peptide synthesis building block. | ||||||||||||||||||||
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References
- [1]. Khan SA, et al. Synthesis of the dodecapeptide-alpha mating factor of Saccharomyces cerevisiae. International journal of peptide and protein research. 1981 Feb;17(2):219-30. [Content Brief]
- [2]. Yasuhiro Nishiyama, et al. Part 42. Application of the 2-adamantyloxycarbonyl (2-Adoc) group to the protection of the imidazole function of histidine in peptide synthesis. J. Chem. Soc., Perkin Trans. 1 1995; 24 (18): 2309-2313.
Keywords
