Description Hmb protection of amide bonds has been shown to inhibit aggregation of ′difficult′ peptides, thereby leading to products of increased purity [1-6]. Retention of Hmb groups on the cleaved peptide can greatly improve the solubility of protected peptide fragments [7, 8] and otherwise intractable sequences [9-11]. Furthermore, using a Hmb protected derivative for incorporation of the residue linked to the carboxyl group of Asp or Asn residues has been found to suppress formation of aspartimide and piperidide related by-products [12-14]. For a comparison of the efficiency of Hmb and pseudoprolines in preventing aggregation, see [15].The product number for this product was previously 04-12-1134..
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Fmoc-(FmocHmb)Val-OH
CAS number:148515-86-0 molecular formula:C43H39NO8
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compound introduction
Specs
| Chinese alias | - | ||
| English alias | BCP07530 | SCHEMBL1740093 | N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[[2-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy]-4-methoxyphenyl]methyl]-L-valine | Fmoc-(Fmoc-Hmb)-Val-OH | FMOC-(FMOCHMB)VAL-OH | HY-W142135 | N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-(2-(((( | ||
| CAS number | 148515-86-0 | molecular formula | C43H39NO8 |
| molecular weight | 697.77 g/mol | Exact mass | ≥98% |
| PSA | 112.000 Ų | logp | 8.9 |
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MSDS
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148515-86-0 | Fmoc-(FmocHmb)Val-OH Novabiochem®.pdf





