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Merck
CN

38904

1,3-Bis(cyanomethyl)imidazolium chloride

purum, ≥98.5% (HPLC/T)

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About This Item

Empirical Formula (Hill Notation):
C7H7ClN4
CAS Number:
Molecular Weight:
182.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥98.5% (HPLC/T)
Form:
powder
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InChI key

PZSHHOPVYJHGQL-UHFFFAOYSA-M

SMILES string

[Cl-].N#CCn1cc[n+](CC#N)c1

InChI

1S/C7H7N4.ClH/c8-1-3-10-5-6-11(7-10)4-2-9;/h5-7H,3-4H2;1H/q+1;/p-1

grade

purum

assay

≥98.5% (HPLC/T)

form

powder

General description

Nitrile-functionalized ionic liquid showing superior characteristics in Suzuki and Stille coupling reactions.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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N Parveen et al.
Soft matter, 13(10), 1988-1997 (2017-02-12)
Controlling the uptake of specific ions in polyelectrolyte multilayers is of interest for various fields of application. Here, we quantify the amount of cation of an ionic liquid, namely 1,3-bis(cyanomethyl)imidazolium chloride, incorporated into polyelectrolyte multilayers upon contact with an ionic
Dongbin Zhao et al.
Journal of the American Chemical Society, 126(48), 15876-15882 (2004-12-02)
A series of relatively low-cost ionic liquids, based on the N-butyronitrile pyridinium cation [C(3)CNpy](+), designed to improve catalyst retention, have been prepared and evaluated in Suzuki and Stille coupling reactions. Depending on the nature of the anion, these salts react

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