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357952

Sigma-Aldrich

1-Isoquinolinecarbonitrile

99%

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About This Item

Empirical Formula (Hill Notation):
C10H6N2
CAS Number:
1198-30-7
Molecular Weight:
154.17
MDL number:
MFCD00134166
UNSPSC Code:
12352100
PubChem Substance ID:
24861952
NACRES:
NA.22

assay

99%

mp

90-92 °C (lit.)

SMILES string

N#Cc1nccc2ccccc12

InChI

1S/C10H6N2/c11-7-10-9-4-2-1-3-8(9)5-6-12-10/h1-6H

InChI key

HJHXYSBRTVFEDD-UHFFFAOYSA-N

General description

Effect of magnetic field on the photosubstitution reaction of 1-isoquinolinecarbonitrile in ethanol has been reported. Conjugated polynitrile, plasma-polymerized 1-isoquinolinecarbonitrile (PPIQCN) has been prepared by plasma polymerization.

Application

1-Isoquinolinecarbonitrile may be used as starting reagent in the syntheses of imidazo[5,1-a]isoquinolines.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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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Synthesis, characterization and optical property of novel conjugated polynitrile.
Zhao X-Y, et al.
Plasma Processes and Polymers, 3(4-5), 333-337 (2006)
Sharmistha Dutta Choudhury et al.
The journal of physical chemistry. B, 110(17), 8850-8855 (2006-04-28)
Laser flash photolysis and an external magnetic field have been used for the study of the interaction of 4-nitroquinoline-1-oxide (4NQO) with some indole derivatives, amino acids, tyrosine and tryptophan, and model proteins, lysozyme and bovine serum albumin. In an aprotic
Kondensierte Isochinoline, XI. Imidazo [5, 1-a] isochinoline.
Reimlinger H, et al.
Chemische Berichte, 108(12), 3771-3779 (1975)
Tamara Rodríguez-Cabo et al.
Analytical and bioanalytical chemistry, 407(20), 6159-6170 (2015-06-05)
Time-of-flight accurate mass spectrometry (TOF-MS), following a previous chromatographic (gas or liquid chromatography) separation step, is applied to the identification and structural elucidation of quinoline-like alkaloids in honey. Both electron ionization (EI) MS and positive electrospray (ESI+) MS spectra afforded

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