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Key Documents

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

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Articles

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.

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

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