75942-39-1

Basic information

• Product Name: 3 6-DIOCTYLOXY-1 2-BENZENEDICARBONITRIL&
• Synonyms: 3 6-DIOCTYLOXY-1 2-BENZENEDICARBONITRIL&
• CAS NO: 75942-39-1
• Molecular Formula: C₂₄H₃₆N₂O₂
• Molecular Weight: 384.55484
• Mol File: 75942-39-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 143-147℃
• Boiling Point: 537.6°C at 760 mmHg
• Flash Point: 185.3°C
• Appearance: /
• Density: 1g/cm³
• Vapor Pressure: 1.25E-11mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: 3 6-DIOCTYLOXY-1 2-BENZENEDICARBONITRIL&(CAS DataBase Reference)
• NIST Chemistry Reference: 3 6-DIOCTYLOXY-1 2-BENZENEDICARBONITRIL&(75942-39-1)
• EPA Substance Registry System: 3 6-DIOCTYLOXY-1 2-BENZENEDICARBONITRIL&(75942-39-1)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22
• Safety Statements: 36
• Hazardous Substances Data: 75942-39-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C24H36N2O2/c1-3-5-7-9-11-13-17-27-23-15-16-24(22(20-26)21(23)19-25)28-18-14-12-10-8-6-4-2/h15-16H,3-14,17-18H2,1-2H3

Upstream product

• 629-27-6 1-Iodooctane 
• 4733-50-0 2,3-dicyano-1,4-hydroquinone 
• 106-51-4 p-benzoquinone 
• 111-83-1 1-bromo-octane 

Downstream Products

• 1356547-10-8 1,4,8,11,15,18-hexaoctyloxy-22,23,24,25-tetrachlorophthalocyanine 
• 1356547-11-9 1,4,15,18-tetraoctyloxy-8-,9,10,11,22,23,24,25-octachlorophthalocyanine 
• 1356547-12-0 1,4,8,11-tetraoctylooxy-15,16,17,18,22,23,24,25-octachlorophthalocyanine 
• 1415139-35-3 C₄₈H₃₈Cl₁₂N₈O₂ 
• 28888-81-5 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecachlorophthalocyanine 
• 1382918-01-5 (Z)-N-((Z)-1-(4-n-butylphenylimino)-4,7-bis(n-octyloxy)isindolin-3-ylidene)-4-butylbenzeneamine 

Relevant articles and documents

Synthesis and spectral properties of unsymmetrical phthalocyanines from 3,6-dioctyloxyphthalonitrile and 3,4,5,6-Tetrachlorophthalonitrile

The random condensation of 3,6-dioctyloxyphthalonitrile (component A) with 3,4,5,6-tetrachlorophthalonitrile (component B) results in unsymmetrical phthalocyanines of A3B, ABAB, and AABB types. Their spectral properties were studied. Pleiades Publishing, Ltd., 2012.

Octa-alkoxy Phthalocyanine and Naphthalocyanine Derivatives: Dyes with Q-band Absorption in the Far Red or Near Infrared

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.