116453-81-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Nitrile compounds are organic compounds that contain a carbon-nitrogen triple bond (C≡N).
Explanation
Dinitriles are a type of nitrile compound that contains two carbon-nitrogen triple bonds.
Explanation
Functional groups are specific groups of atoms within molecules that are responsible for the characteristic chemical reactions of those molecules.
Explanation
As an intermediate, this compound is used in the synthesis of various substances, which can be further processed to create the final products.
Explanation
Due to its unique chemical structure and properties, this compound may be useful in the development of new polymers and materials with specific characteristics.
Explanation
Handling this compound requires caution, as it may pose health risks or environmental hazards if not managed according to safety protocols.
Explanation
Most organic compounds with a large molecular size and complexity tend to be solids at room temperature due to strong intermolecular forces.
Explanation
The presence of nonpolar aromatic rings and hydrophobic groups in the molecule suggests that it may dissolve in organic solvents.
Explanation
Most organic compounds are stable under normal conditions, but their stability can be affected by extreme conditions, which may cause decomposition or chemical reactions.
Chemical class
Nitrile compound
Subclass
Dinitriles
Functional groups
Carbonitrile (CN) and phenylpropoxy (C6H5-CH2-CH2-CH2-O-)
Applications
Intermediate in the production of pharmaceuticals, agrochemicals, and dyes
Potential applications
Polymer synthesis and materials science
Safety concerns
Harmful effects if not properly managed and controlled
Physical state
Likely a solid at room temperature (based on molecular size and complexity)
Solubility
Likely soluble in organic solvents (e.g., acetone, ethanol, or dichloromethane)
Stability
Stable under normal conditions, but may decompose or react under extreme conditions (e.g., high temperature, strong acids or bases)
Check Digit Verification of cas no
The CAS Registry Mumber 116453-81-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,5 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116453-81:
(8*1)+(7*1)+(6*6)+(5*4)+(4*5)+(3*3)+(2*8)+(1*1)=117
117 % 10 = 7
So 116453-81-7 is a valid CAS Registry Number.
116453-81-7Relevant articles and documents
Octa-alkoxy Phthalocyanine and Naphthalocyanine Derivatives: Dyes with Q-band Absorption in the Far Red or Near Infrared
Cook, Michael J.,Dunn, Adrian J.,Howe, Steven D.,Thomson, Andrew J.,Harrison, Kenneth J.
, p. 2453 - 2458 (2007/10/02)
The lithium alkoxide-catalysed cyclic tetramerisation of various 3,6-dialkoxy-4,5-dichlorophthalonitriles, 1,4-dialkoxynaphthalene-2,3-dicarbonitriles and 3,6-dialkoxyphthalonitriles to give the corresponding metal-free octa-alkoxyoctachlorophthalocyanines, octa-alkoxynaphthalocyanines and octa-alkoxyphthalocyanines is described.An unexpected trans-alkoxylation reaction occurs during the cyclisation of the first two series of precursors.Metal-free phthalocyanines and naphthalocyanines have been converted into derivatives containing various metal ions.Compounds show Q-band absorption in the region 739-862 nm in toluene solution.The fluorescence spectra of selected examples are reported.The solubility of some of the compounds has been measured in a formulation of liquid crystal materials.
