670340
Fmoc-pentafluoro-L-phenylalanine
≥97%
Synonym(s):
(S)-2-(Fmoc-amino)-3-(pentafluorophenyl)propionic acid
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About This Item
Empirical Formula (Hill Notation):
C24H16F5NO4
CAS Number:
Molecular Weight:
477.38
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Quality Level
assay
≥97%
optical activity
[α]/D -20.5±1.0°, c = 1 in methanol
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
OC(=O)[C@H](Cc1c(F)c(F)c(F)c(F)c1F)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI
1S/C24H16F5NO4/c25-18-15(19(26)21(28)22(29)20(18)27)9-17(23(31)32)30-24(33)34-10-16-13-7-3-1-5-11(13)12-6-2-4-8-14(12)16/h1-8,16-17H,9-10H2,(H,30,33)(H,31,32)/t17-/m0/s1
InChI key
DLOGILOIJKBYKA-KRWDZBQOSA-N
hcodes
Hazard Classifications
Aquatic Chronic 4
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Lee Schnaider et al.
ACS applied materials & interfaces, 11(24), 21334-21342 (2019-05-29)
The rapid advancement of peptide- and amino-acid-based nanotechnology offers new approaches for the development of biomedical materials. The utilization of fluorenylmethyloxycarbonyl (Fmoc)-decorated self-assembling building blocks for antibacterial and anti-inflammatory purposes represents promising advancements in this field. Here, we present the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 670340-500MG | 04061832595535 |