ALD00374
L-Fmoc-3-fluorophenylalanine
Synonym(s):
Fmoc-Phe(3-F)-OH, Fmoc-3-fluoro-L-phenylalanine
About This Item
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form
solid
Quality Level
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
color
beige
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
FC1=CC=CC(C[C@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)=C1
InChI
1S/C24H20FNO4/c25-16-7-5-6-15(12-16)13-22(23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1
InChI key
DWSDVARCJDOADL-QFIPXVFZSA-N
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Application
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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The Yu program centers around the discovery of catalytic carbon–carbon and carbon–heteroatom bond forming reactions based on C–H activation. Target transformations are selected to enable 1) the use of simple and abundant starting materials such as aliphatic acids, amines and alcohols, and 2) disconnections that drastically shorten the synthesis of a drug molecule or a major class of biologically active compounds.
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