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Merck
CN

12136

1-(3-Cyanopropyl)pyridinium chloride

≥98.5% (T)

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About This Item

Empirical Formula (Hill Notation):
C9H11ClN2
CAS Number:
Molecular Weight:
182.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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assay

≥98.5% (T)

form

solid

impurities

≤0.5% water

mp

130-135 °C

SMILES string

[Cl-].N#CCCC[n+]1ccccc1

InChI

1S/C9H11N2.ClH/c10-6-2-5-9-11-7-3-1-4-8-11;/h1,3-4,7-8H,2,5,9H2;1H/q+1;/p-1

InChI key

VOKQCUHMWFKHFE-UHFFFAOYSA-M

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 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - 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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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
Chunmei Yang et al.
The American journal of pathology, 190(3), 674-688 (2020-01-24)
miRNAs, a well-known group of noncoding RNAs, contribute to the pathogenesis of multiple diseases, including colitis-associated cancer (CAC). Our recent findings indicate that proinflammatory cytokines up-regulate c-MYC level, which subsequently activates cullin 4A and 4B (CUL4A/4B) and CRL4DCAF4 E3 ligases