Description The N-im-Boc group is unstable to prolonged treatment with piperidine [1]; 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. The specific method for the conversion to the free acid is given on page 4.6.The product number for this product was previously 04-12-1110..
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Fmoc-His(Boc)-OH-CHA
CAS number:210820-99-8 molecular formula:C26H27N3O6·C6H13N
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Specs
| Chinese alias | - | ||
| English alias | AS-75059 | Fmoc-L-His(Boc)-OH CHA | Fmoc-His(-Boc)-OH | Fmoc-His(Boc)-OH CHA | cyclohexanamine Na-(((9H-fluoren-9-yl)methoxy)carbonyl)-Nt-(tert-butoxycarbonyl)-L-histidinate | N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-(t-butyloxycarbonyl)-L-histidine cy | ||
| CAS number | 210820-99-8 | molecular formula | C26H27N3O6·C6H13N |
| molecular weight | 576.7 g/mol | Exact mass | ≥98% |
| PSA | 146.000 Ų | logp | - |
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210820-99-8 | Fmoc-His(Boc)-OH.CHA Novabiochem®.pdf





