95865-59-1 Usage
Uses
Used in Catalyst Applications:
(TETRA-T-BUTYLPHTHALOCYANINATO)OXOVANADIUM(IV) is used as a catalyst in various organic reactions due to its redox-active properties and ability to facilitate chemical transformations efficiently.
Used in Electrochemical Devices:
(TETRA-T-BUTYLPHTHALOCYANINATO)OXOVANADIUM(IV) is utilized as a redox-active component in electrochemical devices, where it can participate in electron transfer processes, making it valuable for energy storage and conversion applications.
Used in Solar Energy Conversion and Storage:
(TETRA-T-BUTYLPHTHALOCYANINATO)OXOVANADIUM(IV) has been studied for its potential use in solar energy conversion and storage, capitalizing on its ability to interact with light and participate in redox reactions that can store and release energy.
Used in Pharmaceutical Applications:
Although not explicitly mentioned in the provided materials, given the compound's redox properties and potential biological activity, it could be explored for use in the treatment of certain diseases, where it might act as a therapeutic agent or a diagnostic tool.
Used in Chemical Research:
(TETRA-T-BUTYLPHTHALOCYANINATO)OXOVANADIUM(IV) is also likely to be used in chemical research for studying coordination chemistry, understanding the behavior of vanadium in various oxidation states, and exploring the properties of phthalocyanine complexes.
Check Digit Verification of cas no
The CAS Registry Mumber 95865-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,6 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95865-59:
(7*9)+(6*5)+(5*8)+(4*6)+(3*5)+(2*5)+(1*9)=191
191 % 10 = 1
So 95865-59-1 is a valid CAS Registry Number.
95865-59-1Relevant academic research and scientific papers
Synthesis and properties of tert-butyl-substituted vanadylphthalocyanine dyes
Law, Kock-Yee
, p. 1778 - 1781 (2008/10/08)
Soluble vanadylphthalocyanine dyes of various degree of tert-butyl substitution, (t-Bu)nVOPc, have been synthesized by reacting varying amounts of 4-tert-butylphthalonitrile and phthalonitrile with vanadium trichloride. The number of tert-butyl substituents on the VOPc ring is calculated from the elemental analysis results, which are in good agreement with the 1H NMR data and are compatible with the mass spectrometric results. The solid-state properties of (t-Bu)nVOPc were studied by absorption spectroscopy and the X-ray powder diffraction technique, and results show that, at n = 4.0, the dye molecules form a non-IR-absorbing, amorphous VOPc phase I in the solid state and that, at n = 1.4, the crystalline, IR-absorbing VOPc phase II is formed. These results are discussed in terms of a steric effect on the packing of (t-Bu)nVOPc molecules into the phase II of VOPc in the solid state.
