4,5-Dichlorophthalonitrile structure
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Common Name | 4,5-Dichlorophthalonitrile | ||
|---|---|---|---|---|
| CAS Number | 139152-08-2 | Molecular Weight | 197.021 | |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 312.4±42.0 °C at 760 mmHg | |
| Molecular Formula | C8H2Cl2N2 | Melting Point | 180-184ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 141.1±22.1 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Synthesis of water soluble PEGylated (copper) phthalocyanines via Mitsunobu reaction and Cu (i)-catalysed azide-alkyne cycloaddition (CuAAC) click chemistry. Li M, et al.
Polym. Chem. 4(16) , 4405-4411, (2013)
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A simple synthesis of 4,5-disubstituted 1,2-dicyanobenzenes and 2,3,9,10,16,17,23,24-octasubstituted phthalocyanines. Wohrle D, et al.
Synthesis , 194-196, (1993)
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Synthesis and characterization of novel symmetrical phthalocyanines substituted with mono-or bi-macrocycles. Kandaz M, et al.
Polyhedron 19(1) , 115-121, (2000)
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Discotic liquid crystals of transition metal complexes 37*: a thermotropic cubic mesophase having Pn m symmetry exhibited by phthalocyanine-based derivatives. Ichihara M, et al.
Liq. Cryst. 34(5) , 555-567, (2007)
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A novel route to 4-chloro-5-alkyl-phthalonitrile and phthalocyanines derived from it. Dinçer, HA, et al.
J. Porphyr. Phthalocyanines 8(10) , 1204-1208, (2004)
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Sterically demanded unsymmetrical zinc phthalocyanines for dye-sensitized solar cells. Giribabu L, et al.
Dyes and Pigments 98(3) , 518-529, (2013)
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Synthesis of sulfonamide-substituted phthalocyanines. Carvalho EFA, et al.
Tetrahedron Lett. 50(49) , 6882-6885, (2009)
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