184359-29-3

Upstream product

• 31643-49-9 4-Nitrophthalonitrile 
• 99-96-7 4-hydroxy-benzoic acid 
• 85218-66-2 4-(4-hydroxycarbonylphenoxy)phthalonitrile 

Downstream Products

• 919766-66-8 4-(4-pentyloxycarbonylphenoxy)phthalonitrile 
• 942492-94-6 (CH₃)2CHCH₂CH₂OOCC₆H₄OC₆H₃(CN)2 
• 942492-95-7 CH₃(CH₂)5OOCC₆H₄OC₆H₃(CN)2 
• 942492-97-9 CH₃(CH₂)7OOCC₆H₄OC₆H₃(CN)2 
• 942492-98-0 CH₃(CH₂)8OOCC₆H₄OC₆H₃(CN)2 

Relevant academic research and scientific papers

Phthalonitriles containing ester groups and copper phthalocyanines based on them

Phthalonitriles containing ester groups were obtained by acylation of 4-hydroxyphthalonitrile and esterification of 4-(p-carboxyphenyloxy) phthalonitriles. On the basis of these phthalonitriles the respective copper phthalocyanines were synthesized. Spectral and some other physical and chemical properties of the synthesized compounds were investigated.

Copper 2,9(10),16(17),23(24)- and 1,8(11),15(18),22(25)-tetra-(4- carboxyphenoxy)phthalocyanines and their esters: The synthesis and liquid-crystalline properties

Copper 2,9(10),16(17),23(24)- and 1,8(11),15(18),22(25)-tetra(4- carboxyphenoxy)phthalocyanines and their carboxylic esters were synthesized and their spectral characteristics and liquid-crystalline properties were studied. 2,9(10),16(17),23(24)-Tetrasubs

Mesomorphism and glass formation of phthalocyanine metal complexes with bulky substituents

This paper deals with the synthesis of phthalocyanine complexes, containing four oligo(oxyethylene)-, oxybenzene-, esther of p-oxybenzoic acid or p-oxyazobenzene side chains terminated by a bulky trityl substituent. Their purity was established by column