86723-23-1

Usage

Explanation

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

Explanation

OCBA is a shorter, more convenient name used to refer to 1,2-Benzenediamine, 4,5-bis(octyloxy)-.

Explanation

This describes the color and form of the compound in its solid state.
4. Chemical compound

Explanation

OCBA is a chemical compound, meaning it is a substance formed from two or more elements chemically bonded together.
5. Crosslinking agent

Explanation

OCBA is used as a crosslinking agent in the production of polymers, which helps to improve their mechanical and thermal properties.
6. Applications in polymer production

Explanation

OCBA is particularly used in the manufacturing of liquid crystal displays and other electronic devices, enhancing the performance of the materials used.
7. High-performance materials

Explanation

The improved mechanical and thermal properties of polymers with OCBA make them suitable for high-performance applications.
8. Organic chemistry applications

Explanation

This describes the arrangement of atoms and functional groups within the molecule, which contributes to its properties and applications.

Physical appearance

Light yellow to brownish powder

Chemical structure

1,2-Benzenediamine with two octyloxy groups attached to the 4,5 positions

Upstream product

• 156777-91-2 1,2-bis(octyloxy)-4,5-dinitrobenzene 
• 111-83-1 1-bromo-octane 
• 120-80-9 benzene-1,2-diol 
• 4956-41-6 1,2-dioctyloxybenzene 

Downstream Products

• 1018902-81-2 C₃₄H₆₀N₂O₃ 
• 1018902-83-4 C₄₂H₇₆N₂O₃ 
• 1018902-84-5 C₄₆H₇₆N₂O₃ 
• 308124-74-5 1,2-dioctyloxy-4-[3'-oxo-3'-(2'',3'',4''-trioctyloxyphenyl)-1'-propenylamino]-5-aminobenzene 
• 1380685-10-8 diethyl (2E,2'E)-2,2'-{[4,5-bis(octyloxy)-1,2-phenylene]bis[imino-(E)-methylylidene]}bis(3-oxobutanoate) 
• 1597409-61-4 (E,E)[{dimethyl-2,2'[4,5-dioctyloxy-1,2-phenylenebis(iminomethylidyne)]bis-3-oxobutanato}] 
• 1192352-08-1 4,7-dibromo-5,6-bis(octyloxy)benzo-[c][1,2,5]-thiadiazole 
• 1254353-37-1 5,6-bis(octyloxy)benzo[c][1,2,5]thiadiazole 
• 944831-68-9 C₆₈H₁₁₀N₂O₆ 

Relevant academic research and scientific papers

Molecular Coplanarity and Self-Assembly Promoted by Intramolecular Hydrogen Bonds

Active conformational control is realized in a conjugated system using intramolecular hydrogen bonds to achieve tailored molecular, supramolecular, and solid-state properties. The hydrogen bonding functionalities are fused to the backbone and precisely pr

Spectroscopic and theoretical optical properties of indoleninyl-substituted dibenzotetraaza[14]annulenes

Two new macrocyclic dibenzotetraaza[14]annulene (DBTAA) compounds with indolenine (5) and pyridoindolenine (6) moieties were synthesized and characterized by spectroscopy. Both DBTAAs exhibit strong UV-Vis absorption properties in the Soret band region. T

A Constrained and “Inverted” [3+3] Salphen Macrocycle with an ortho-Phenylethynyl Substitution Pattern

A [3+3] Schiff-base salphen macrocycle (7 a) was synthesized by imine condensation between ortho-phenylenediamine and ortho-phenylethynyl-bridged bis(5-salicylaldehyde) precursors. The triangular-shaped macrocycle 7 a has a nonclassical (or “inverted”) de

Constructing a self-assembling C3-symmetric covalently linked (fused) donor-acceptor-type molecule containing a hexaazatriphenylene core

A C3-symmetric covalently linked (fused) molecule, HAT-IPN, comprising a 13 fused ring system was synthesized by a condensation-cyclisation reaction between hexaazatriphenylenehexacarboxylic acid trisanhydride and 4,5-diamino-1,2-dioctyloxybenzene. This fused system exhibits ambipolar behaviour due to an n-type HAT-core at the center and three outer p-type fused dialkoxybenzimidazole moieties, which is confirmed by cyclic voltammetry. The self-assembling nature of this disc-shaped donor-acceptor type system is evident in13C NMR spectroscopy, dynamic light scattering studies, differential scanning calorimetry and atomic force microscopy (AFM) images, which illustrate the formation of the one-dimensional aggregates both in solution and in the film state; indicating its potential as an active component in organic electronic devices.

Amphiphilic iron(ii) complexes with short alkyl chains-crystal packing and spin transition properties

An amphiphilic iron(ii) spin crossover complex with relatively short octyl chains was synthesised and the crystal structures of the high spin and the low spin state could be determined. In further reactions, a second modification of the hexa-coordinated c

Fluoro-functionalization of vinylene units in a polyarylenevinylene for polymer solar cells

A low band-gap copolymer PDTBTFV alternating bis-thienyl-(bis-alkoxy)- benzothiadiazole blocks with difluorovinylene units and its non-fluorinated counterpart PDTBTV have been synthesized and characterized as donor materials in bulk heterojunction (BHJ) s

New octahedral, head-tail iron(II) complexes with spin crossover properties

The synthesis and characterisation of four new Schiff base-like ligands with long alkyl chains in the outer periphery and their iron(II) complexes with methanol and pyridine as axial ligands is reported. Two of the methanol complexes crystallise in a lipi

Capsule formation in novel cadmium cluster metallocavitands

We report the synthesis and characterization of a new heptanuclear cadmium cluster complex formed within a Schiff base macrocycle and study its surprising dimerization in the solid-state and solution to form capsules. The Royal Society of Chemistry.

In Situ Synthesis of Hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′ -c]phenazines: Mesogenic Phase Transition of the Electron-Deficient Discotic Compounds

2,3,8,9,14,15-Hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′- c]phenazines with alkyl side chains varying from 6 to 12 carbon atoms were readily synthesized by the condensation of hexaketocyclohexane with the respective 1,2-bisalkoxy-4,5-diaminobenzene. Polariz