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About This Item
Empirical Formula (Hill Notation):
C5H3BCl2F5N
CAS Number:
Molecular Weight:
253.79
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
427-400-1
MDL number:
Assay:
97%
InChI key
JVYBYXWHPIEUOT-UHFFFAOYSA-N
InChI
1S/C5H3Cl2FN.BF4/c6-4-2-1-3-5(7)9(4)8;2-1(3,4)5/h1-3H;/q+1;-1
SMILES string
F[B-](F)(F)F.F[n+]1c(Cl)cccc1Cl
assay
97%
mp
212-215 °C (lit.)
functional group
chloro
Quality Level
General description
2,6-Dichloro-1-fluoropyridinium tetrafluoroborate is widely employed as fluorinating reagent in various reactions.
Application
2,6-Dichloro-1-fluoropyridinium tetrafluoroborate may be employed for the regioselective fluorination of fluorene.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
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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Fluorination of fluorene, dibenzofuran and their open analogues with caesium fluoroxysulfate and related fluorinating reagents.
Iskra J, et al.
Collection of Czechoslovak Chemical Communications, 73(12), 1671-1680 (2008)
Electrophilic NF Fluorinating Agents.
G. Sankar Lal et al.
Chemical reviews, 96(5), 1737-1756 (1996-08-01)
Oriol Planas et al.
Science (New York, N.Y.), 367(6475), 313-317 (2020-01-18)
Bismuth catalysis has traditionally relied on the Lewis acidic properties of the element in a fixed oxidation state. In this paper, we report a series of bismuth complexes that can undergo oxidative addition, reductive elimination, and transmetallation in a manner
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