1,3-dicyclohexylimidazol-1-ium;tetrafluoroborate

Names

[ Name ]:
1,3-dicyclohexylimidazol-1-ium;tetrafluoroborate

[Synonym ]:
1,3-DicyclohexyliMidazoliuM Tetrafluoroborate
1,3-Dicyclohexylimidazolium tetrafluoroborate salt
1,3-Dicyclohexyl-1H-imidazol-3-ium tetrafluoroborate
1,3-Bis(cyclohexyl)imidazolium tetrafluoroborate

Chemical & Physical Properties

[ Melting Point ]:
171-175ºC

[ Molecular Formula ]:
C₁₅H₂₅BF₄N₂

[ Molecular Weight ]:
320.177

[ Exact Mass ]:
320.204681

[ PSA ]:
8.81000

[ LogP ]:
5.08600

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933290090

Customs

[ HS Code ]: 2933290090

[ Summary ]:
2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Efficient C-B bond formation promoted by N-heterocyclic carbenes: synthesis of tertiary and quaternary B-substituted carbons through metal-free catalytic boron conjugate additions to cyclic and acyclic alpha,beta-unsaturated carbonyls.

J. Am. Chem. Soc. 131th ed.,, 7253, (2009)

Metal-free nucleophilic activation of a B-B bond has been exploited in the development of a highly efficient method for conjugate additions of commercially available bis(pinacolato)diboron to cyclic o...