47475
Fmoc-Pro-OPfp
≥96.0%
Synonym(s):
N-(9-Fluorenylmethoxycarbonyl)-L-proline pentafluorophenyl ester, Fmoc-L-proline pentafluorophenyl ester
About This Item
Recommended Products
Assay
≥96.0%
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
127-129 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
Fc1c(F)c(F)c(OC(=O)[C@@H]2CCCN2C(=O)OCC3c4ccccc4-c5ccccc35)c(F)c1F
InChI
1S/C26H18F5NO4/c27-19-20(28)22(30)24(23(31)21(19)29)36-25(33)18-10-5-11-32(18)26(34)35-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2/t18-/m0/s1
InChI key
CQBLOHXKGUNWRV-SFHVURJKSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
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Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
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