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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signalword
Warning
hcodes
pcodes
Hazard Classifications
Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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Articles
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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