171719
1,2-Dicyanobenzene
98%
Synonym(s):
Phthalonitrile
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About This Item
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Quality Level
Assay
98%
form
solid
mp
137-139 °C (lit.)
functional group
nitrile
SMILES string
N#Cc1ccccc1C#N
InChI
1S/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H
InChI key
XQZYPMVTSDWCCE-UHFFFAOYSA-N
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Application
1,2-Dicyanobenzene was used in the synthesis of a six-coordinate phthalocyanine analogue.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 3
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Dalton transactions (Cambridge, England : 2003), 42(47), 16486-16489 (2013-10-18)
A reaction of 1,2-dicyanobenzene and lithium methoxide at 70 °C in methanol yielded the half-phthalocyanine intermediate, which coordinates to a cadmium(II) ion in the subsequent reaction step to give the first example of a six-coordinate phthalocyanine analogue containing a divalent
Guang pu xue yu guang pu fen xi = Guang pu, 29(1), 207-210 (2009-04-24)
In decades, metallo-phthalocyanines (MPcs) have undergone a renaissance because of their singular and unconventional physical properties. However, for the successful application of MPcs in practical devices, it is important to disperse MPc molecules into solid state matrix to fabricate MPc
Theranostics, 9(22), 6412-6423 (2019-10-08)
Targeted delivery of therapeutic agents is of particular interest in the field of cancer treatment. However, there is an urgent need for developing clinically promising targeting approaches that can be readily administered in a green manner. Methods: Five phthalocyanine derivatives
An estimation of the sublimation rate of o-phthalodinitrile and acrylamide during filter sampling.
Industrial health, 23(2), 167-170 (1985-01-01)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 53A(12), 2033-2039 (1998-01-23)
A zero-order normal coordinate analysis was made for p-, m- and o-dicyanobenzenes and their deuterated isomers by transferring the force constants from Part I. The observed and calculated frequencies agree with an average error of 18.7 cm-1, demonstrating the transferability
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