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47474

Sigma-Aldrich

Fmoc-Phe-OPfp

≥96.0%

Synonym(s):

N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine pentafluorophenyl ester, Fmoc-L-phenylalanine pentafluorophenyl ester

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About This Item

Empirical Formula (Hill Notation):
C30H20F5NO4
CAS Number:
Molecular Weight:
553.48
Beilstein:
4241247
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.26

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

SMILES string

Fc1c(F)c(F)c(OC(=O)[C@H](Cc2ccccc2)NC(=O)OCC3c4ccccc4-c5ccccc35)c(F)c1F

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

InChI key

WKHPSOMXNCTXPK-QFIPXVFZSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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