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Thermo Scientific Chemicals
Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate, 98%
CAS: 164298-23-1 | C5H12F7N2P | 264.128 g/mol
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Chemical Identifiers
CAS164298-23-1
IUPAC Name[(dimethylamino)(fluoro)methylidene]dimethylazanium
Molecular FormulaC5H12FN2
InChI KeyJILUGXGJYPRQPA-UHFFFAOYSA-N
SMILESCN(C)C(F)=[N+](C)C
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)>97.5%
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Suitable for battery materials development.
Applications
Fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate is used as a reagent for synthesis of cationic antimicrobial β-2,2-amino acid derivatives, philanthotoxin analogues for inhibition of the ionotropic glutamate receptor, small β-peptidomimetics for antimicrobials and hydrazone ligation to assemble multifunctional viral nanoparticles.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
Fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate is used as a reagent for synthesis of cationic antimicrobial β-2,2-amino acid derivatives, philanthotoxin analogues for inhibition of the ionotropic glutamate receptor, small β-peptidomimetics for antimicrobials and hydrazone ligation to assemble multifunctional viral nanoparticles.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Terkel Hansen.; Dominik Ausbacher.; Gøril E Flaten.; Martina Havelkova.; Morten B Strom. Synthesis of cationic antimicrobial β(2,2)-amino acid derivatives with potential for oral administration. Journal of medicinal and pharmaceutical chemistry. 2011, 54 (3), 858-868.
- Sidsel Frolund.; Angelo Bella.; Anders S Kristensen.; Hanne L Ziegler.; Matthias Witt.; Christian A Olsen.; Kristian Stromgaard.; Henrik Franzyk.; Jerzy W Jaroszewski. Assessment of structurally diverse philanthotoxin analogues for inhibitory activity on ionotropic glutamate receptor subtypes: discovery of nanomolar, nonselective, and use-dependent antagonists. Journal of medicinal and pharmaceutical chemistry. 2010, 537 (20), 7441-7451.