47834
Fmoc-D-Phe(4-CF3)-OH
≥98.0%
Synonym(s):
Fmoc-4-(trifluoromethyl)-D-phenylalanine
Sign In to View Organizational & Contract Pricing.
About This Item
Empirical Formula (Hill Notation):
C25H20F3NO4
CAS Number:
Molecular Weight:
455.43
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
assay
≥98.0%
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](Cc1ccc(cc1)C(F)(F)F)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI
1S/C25H20F3NO4/c26-25(27,28)16-11-9-15(10-12-16)13-22(23(30)31)29-24(32)33-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14H2,(H,29,32)(H,30,31)/t22-/m1/s1
InChI key
YMEGJWTUWMVZPD-JOCHJYFZSA-N
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Fayçal Touti et al.
Nature chemical biology, 15(4), 410-418 (2019-03-20)
The use of competitive inhibitors to disrupt protein-protein interactions (PPIs) holds great promise for the treatment of disease. However, the discovery of high-affinity inhibitors can be a challenge. Here we report a platform for improving the affinity of peptide-based PPI
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 47834-1G | 04061826102046 |