Abstract
3,5-Dimethoxy-2-[(4-methoxyphenyl)diazenyl]phenol was synthesized by an azo-coupling reaction between 3,5-dimethoxyphenol and 4-methoxy benzenediazonium tetrafluoroborate. The structure of newly synthesized compound was elucidated based on 1H NMR, 13C NMR, ESI-MS, UV-Vis and FT-IR.
Highlights
The stRreuccetivuerde: 1o6fJunlye2w02l0y; Ascycenptthede:s6izAeudgucsot 2m02p0;oPuunbldishweda: s11eAluugcuidsta2t0e2d0 based on 1H NMR, 13C NMR, ESI-MS, UV-Vis and FT-IR
3,5-Dimethoxy-2-[(4-methoxyphenyl)diazenyl]phenol was synthesized by an Keywoatezrtodra-scf:oluuboperlnoinbzgoernaetrede.aiacTtzhiooennsiturbumecttwsuareleetn;o3f,53n,e5dw-idmliymesetyhthnootxhxyeysppizhheeednnooclol;maapznoodu-cnod4u-mwpelaitsnhogexluryecaidcbateitneodznenbeadseiadzoonniu1mH
A1z.oInctoromdpucotuionnds are a well-known class of compounds widely used in industry as colorants in textile, cosmetics, and paper-printing fields [1,2]
Summary
A1z.oInctoromdpucotuionnds are a well-known class of compounds widely used in industry as colorants in textile, cosmetics, and paper-printing fields [1,2]. DeparSthmoretnNt ootfeIndustrial Chemistry “Toso Montanari”, Alma Mater Studiorum—Università di Bologna, The stRreuccetivuerde: 1o6fJunlye2w02l0y; Ascycenptthede:s6izAeudgucsot 2m02p0;oPuunbldishweda: s11eAluugcuidsta2t0e2d0 based on 1H NMR, 13C NMR, ESI-MS, UV-Vis and FT-IR. Abstract: 3,5-Dimethoxy-2-[(4-methoxyphenyl)diazenyl]phenol was synthesized by an Keywoatezrtodra-scf:oluuboperlnoinbzgoernaetrede.aiacTtzhiooennsiturbumecttwsuareleetn;o3f,53n-,e5dw-idmliymesetyhthnootxhxyeysppizhheeednnooclol;maapznoodu-cnod4u-mwpelaitsnhogexluryecaidcbateitneodznenbeadseiadzoonniu1mH
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