38791-69-4

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The color and physical state of the compound, which can be useful for identification and handling purposes.

Explanation

This property indicates the compound's ability to dissolve in different types of solvents, which can be important for its use in various applications.

Explanation

The chemical structure provides information about the arrangement of atoms and functional groups within the molecule, which can influence its reactivity and properties.

Explanation

This property highlights the compound's role as a starting material for the production of other chemicals, which can be used in various industries.

Explanation

The compound's specific structural features and properties make it a potentially important contributor to the creation of new materials and technologies, which can have a wide range of applications.

Appearance

Yellowish-white powder

Solubility

Insoluble in water, soluble in organic solvents

Chemical structure

Contains a 1,2-benzenedicarbonitrile group and a 4,4'-[[1,1'-biphenyl]-4,4'-diylbis(oxy)]bisgroup

Use

Building block in the synthesis of various organic compounds and polymers

Applications

Potential use in plastics, pharmaceuticals, and materials science industries

Unique structure and properties

Valuable component in the development of advanced materials and technologies

Upstream product

• 31643-49-9 4-Nitrophthalonitrile 
• 92-88-6 4,4'-Dihydroxybiphenyl 

Relevant academic research and scientific papers

Polymerizable composition

A polymerizable composition, a prepolymer, a phthalonitrile resin, or a composite provided herein has excellent heat resistance and does not cause defects that may adversely affect physical properties. In addition, the polymerizable composition exhibits a

Phthalonitrile resin

The present application relates to a phthalonitrile resin and the like. The present application can provide a phthalonitrile resin, and a polymerizable composition and prepolymer using the same, which can exhibit excellent curability, a suitable processin

PHTHALONITRILE COMPOUND

The present application can provide a phthalonitrile compound and a use thereof. The present application can provide a phthalonitrile compound capable of forming a phthalonitrile resin by self-curing or of serving as a curing agent after being mixed with

PHTHALONITRILE COMPOUND

The present application relates to a novel phthalonitrile compound and a use thereof. The phthalonitrile compound has a novel structure and can exhibit excellent effects in a use known for which a phthalonitrile compound can be applied. The use of the pht

PHTHALONITRILE COMPOUND

The present application can provide a phthalonitrile compound and a use thereof. The phthalonitrile compound has a novel structure, and can exhibit an excellent effect in a use to which the phthalonitrile compound can be applied. An example of the use of

Phthalonitrile compound

The present invention relates to a phthalonitrile compound represented by chemical formula 1 and a phthalonitrile resin obtained therefrom, a polymerizable composition, a prepolymer, a complex and a method for manufacturing the complex. The phthalonitrile

A phthalocyanine material binuclear Asia method for the preparation of

The invention provides a preparation method of a di-nuclear sub-phthalocyanine substance. The preparation method specifically comprises the following steps of: firstly, performing a nucleophilic substitution reaction on the 4-nitro phthalonitrile as start

Phthalonitrile compound

The present invention relates to a novel phthalonitrile compound and use thereof. The phthalonitrile compound has a novel structure and can provide excellent effects in the known uses to which phthalonitrile compounds can be applied. The phthalonitrile co

Polyphthalocyanine resins

The synthesis and subsequent polymerization of highly aromatized phthalonile monomers which contain phenoxy linkages having a substantially aromatic spacer moiety between the two terminal phthalonitrile groups is disclosed. The phthalonitriles are synthe

Aromatic bis(ether phthalis anhydride) compounds

Aromatic bis(ether anhydride)s are prepared from the hydrolysis of the reaction product of a nitro-substituted phenyl dinitrile with a metal salt of a dihydroxy aryl compound in the presence of a dipolar aprotic solvent.