357952
1-Isoquinolinecarbonitrile
99%
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About This Item
Empirical Formula (Hill Notation):
C10H6N2
CAS Number:
Molecular Weight:
154.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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.
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
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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Synthesis, characterization and optical property of novel conjugated polynitrile.
Zhao X-Y, et al.
Plasma Processes and Polymers, 3(4-5), 333-337 (2006)
Kondensierte Isochinoline, XI. Imidazo [5, 1-a] isochinoline.
Reimlinger H, et al.
Chemische Berichte, 108(12), 3771-3779 (1975)
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