Structure

Fmoc-His(Boc)-OH-CHA

CAS
210820-99-8
Catalog Number
ACM210820998-1
Category
Amino Acids
Molecular Weight
477.51

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Specification

Description
The N-im-Boc group is unstable to prolonged treatment with piperidine ; the utility of this derivative is therefore limited to the preparation of short sequences by Fmoc SPPS. This derivative is supplied as a CHA-salt.
Synonyms
Fmoc-His(Boc)-OH-CHA, N-α-Fmoc-N-im-t.-Boc-L-histidine cyclohexylammonium salt
InChI
1S/C26H27N3O6.C6H13N/c1-26(2,3)35-25(33)29-13-16(27-15-29)12-22(23(30)31)28-24(32)34-14-21-19-10-6-4-8-17(19)18-9-5-7-11-20(18)21;7-6-4-2-1-3-5-6/h4-11,13,15,21-22H,12,14H2,1-3H3,(H,28,32)(H,30,31);6H,1-5,7H2/t22-;/m0./s1
InChI Key
UDEXYAHZNOKVIG-FTBISJDPSA-N
Application
Peptide synthesis.
Assay
≥97% (TLC)
≥97.0% (HPLC)
Form
powder
Functional Group
Boc, Fmoc
Reaction Suitability
reaction type: Fmoc solid-phase peptide synthesis
Storage Temperature
-20℃(-15℃to -25℃)
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