47474
Fmoc-Phe-OPfp
≥96.0%
别名:
N-芴甲氧羰基-L-苯丙氨酸五氟苯酯, Fmoc-L-苯丙氨酸五氟苯酯
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关于此项目
经验公式（希尔记法）:
C30H20F5NO4
化学文摘社编号:
分子量:
553.48
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4241247
InChI
1S/C30H20F5NO4/c31-23-24(32)26(34)28(27(35)25(23)33)40-29(37)22(14-16-8-2-1-3-9-16)36-30(38)39-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,36,38)/t22-/m0/s1
SMILES string
Fc1c(F)c(F)c(OC(=O)[C@H](Cc2ccccc2)NC(=O)OCC3c4ccccc4-c5ccccc35)c(F)c1F
InChI key
WKHPSOMXNCTXPK-QFIPXVFZSA-N
assay
≥96.0%
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
149-151 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
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signalword
Warning
hcodes
pcodes
Hazard Classifications
Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Rebecca M Turk-Macleod et al.
Journal of molecular evolution, 74(3-4), 217-225 (2012-04-28)
According to the RNA world hypothesis, coded peptide synthesis (translation) must have been first catalyzed by RNAs. Here, we show that small RNA sequences can simultaneously bind the dissimilar amino acids His and Phe in peptide linkage. We used in
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