ALD00374
Fmoc-Phe(3-F)-OH
别名:
Fmoc-L-3-氟苯丙氨酸
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关于此项目
经验公式（希尔记法）:
C24H20FNO4
化学文摘社编号:
分子量:
405.42
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
InChI key
DWSDVARCJDOADL-QFIPXVFZSA-N
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
form
solid
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
color
beige
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Quality Level
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Application
Phenylalanine derivative was introduced in collaboration with Yu and coworkers in reflection to a methodology reported in C-H Activation.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
相关内容
Yu program focuses on efficient C–H bond activation for drug synthesis, using simple starting materials.
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