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About This Item
Linear Formula:
[FC[=N(CH3)2]N(CH3)2]PF6
CAS Number:
Molecular Weight:
264.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352107
MDL number:
InChI
1S/C5H12FN2.F6P/c1-7(2)5(6)8(3)4;1-7(2,3,4,5)6/h1-4H3;/q+1;-1
SMILES string
F[P-](F)(F)(F)(F)F.CN(C)\C(F)=[N+](/C)C
InChI key
ZAVXOOLKAGPJPI-UHFFFAOYSA-N
assay
97%
reaction suitability
reaction type: Coupling Reactions
mp
104-109 °C (lit.)
application(s)
peptide synthesis
functional group
amine, fluoro
Quality Level
Application
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
Amine prodrugs of selective neuronal nitric oxide synthase inhibitors
Reagent for:
Selective cyclohexyl-derived imidazopyrazine insulin-like growth factor 1 receptor inhibitors
Hydrazone ligation to assemble multifunctional viral nanoparticles
Cationic antimicrobial β-2,2-amino acid derivatives
Philanthotoxin analogues for inhibition of the ionotropic glutamate receptor
Small β-peptidomimetics for antimicrobials
Amine prodrugs of selective neuronal nitric oxide synthase inhibitors
Reagent for:
Selective cyclohexyl-derived imidazopyrazine insulin-like growth factor 1 receptor inhibitors
Hydrazone ligation to assemble multifunctional viral nanoparticles
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
signalword
Danger
hcodes
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Anita K Kovács et al.
Frontiers in chemistry, 6, 120-120 (2018-05-05)
A general strategy for the synthesis of N-peptide-6-amino-D-luciferin conjugates has been developed. The applicability of the strategy was demonstrated with the preparation of a known substrate, N-Z-Asp-Glu-Val-Asp-6-amino-D-luciferin (N-Z-DEVD-aLuc). N-Z-DEVD-aLuc was obtained via a hybrid liquid/solid phase synthesis method, in which
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