114364-56-6

Basic information

• Product Name: 1,2-Benzenedicarbonitrile, 4,5-bis(dodecyloxy)-
• CAS NO: 114364-56-6
• Molecular Formula: C32H52N2O2
• Molecular Weight: 496.777
• Mol File: 114364-56-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,2-Benzenedicarbonitrile, 4,5-bis(dodecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenedicarbonitrile, 4,5-bis(dodecyloxy)-(114364-56-6)
• EPA Substance Registry System: 1,2-Benzenedicarbonitrile, 4,5-bis(dodecyloxy)-(114364-56-6)

Safety Data

• Hazardous Substances Data: 114364-56-6(Hazardous Substances Data)

Usage

Explanation

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

Explanation

It is a chemical compound derived from benzene, which is a basic structure consisting of a six-carbon ring with alternating single and double bonds.

Explanation

Dodecyloxy side chains are alkyl chains with 12 carbon atoms (C12H25) attached to an oxygen atom (-O-). These chains are present in the compound, providing additional properties to the molecule.

Explanation

Due to its structure, 1,2-Benzenedicarbonitrile, 4,5-bis(dodecyloxy)is used as a starting material for the synthesis of various polymers and materials, contributing to their durability and flexibility.

Explanation

The compound's unique structure makes it suitable as a starting material for the production of various chemicals, including surfactants, lubricants, and other specialty chemicals.

Explanation

The presence of dodecyloxy side chains in the compound makes it suitable for use as a dispersant and wetting agent in various formulations, as these chains can help in the dispersion and wetting of other substances.

Type of compound

Benzene derivative

Functional groups

Two carbonitrile functional groups

Side chains

Two dodecyloxy side chains

Industrial applications

Building block for polymer synthesis

Use as a starting material

Production of surfactants, lubricants, and specialty chemicals

Suitability as a dispersant and wetting agent

Due to dodecyloxy side chains

Upstream product

• 544-92-3 copper(I) cyanide 
• 114364-55-5 1,2-dibromo-4',5'-di-n-dodecyloxybenzene 
• 112-53-8 1-dodecyl alcohol 
• 181144-60-5 1,2-bis(dodecycloxy)-4,5-diiodobenzene 
• 143-15-7 1-dodecylbromide 
• 42244-53-1 1,2-bisdodecyloxybenzene 
• 114364-58-8 1,3-diimino-5,6-bis(dodecyloxy)isoindoline 
• 120-80-9 benzene-1,2-diol 
• 2563-26-0 4,5-dibromobenzene-1,2-diol 

Downstream Products

• 152109-27-8 zinc(II) 2,3,9,10,16,17,23,24-octakis(dodecyloxy)phthalocyaninato^(2-)-N²⁹, N³⁰, N³¹, N³² 

Relevant articles and documents

Synthesis and self-assembly of phthalocyanine-tethered block copolymers

A series of novel phthalocyanine (Pc)-tethered block copolymers, Pc-poly(methyl methacrylate)-block-polystyrene (Pc-PMMA-b-PS), with various molecular weights (number average molecular weight mass = 41, 66, 86 kg mol-1), were prepared by atom transfer radical polymerization and click chemistry. The structurally related Pc-tethered homopolymer, Pc-PMMA was also synthesized for comparison. Pc-PMMA forms homogeneous polymer films containing π-assemblies of the terminal Pc groups, whereas Pc-PMMA-b-PS self-assembles into a cylindrical morphology in which the Pc units show π-π interactions inside the confined PMMA cylinders. Such polymer designs have potential applications in optoelectronic devices. This journal is

SYNTHESIS AND PROPERTIES OF NOVEL OCTASUBSTITUTED METALLOPHTHALOCYANINES

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Control of the Discotic to Isotropic Transition in Alkoxy-Substituted Silicondihydroxo-Phthalocyanines by Axial Substituents

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