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660019

Sigma-Aldrich

1,3-Diisopropylimidazolium tetrafluoroborate

96%

Synonym(s):

1,3-Bis(1-methylethyl)-1H-imidazolium tetrafluoroborate, 1,3-Di-isopropyl-imidazol-2-ylidinium tetrafluoroborate, N,N′-Di-isopropyl-imidazolium tetrafluoroborate

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About This Item

Empirical Formula (Hill Notation):
C9H17N2 · BF4
CAS Number:
Molecular Weight:
240.05
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

96%

form

solid

reaction suitability

reagent type: catalyst

mp

62-79 °C

SMILES string

F[B-](F)(F)F.CC(C)n1cc[n+](c1)C(C)C

InChI

1S/C9H17N2.BF4/c1-8(2)10-5-6-11(7-10)9(3)4;2-1(3,4)5/h5-9H,1-4H3;/q+1;-1

InChI key

PSKQPXYUPOKHPY-UHFFFAOYSA-N

Related Categories

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Articles

A wide range of NHC ligands are commonly available which exhibit high activities.

Rapid progress in cross-coupling reactions of unactivated substrates catalyzed by metal complexes has transformed the chemical market-place through introduction of an extensive library of achiral and chiral phosphine ligands.

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