735270-31-2 Usage
Uses
Used in Pharmaceutical Research:
2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-5-methoxy(9CI) is used as a research compound for exploring its potential biological activities and therapeutic effects. Its unique structure may contribute to the development of new drugs or drug candidates.
Used in Chemical Research:
In the field of chemical research, 2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-5-methoxy(9CI) serves as a valuable compound for studying its chemical properties, reactivity, and potential applications in various chemical processes.
Further research is necessary to fully understand the properties and potential uses of 2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-5-methoxy(9CI), as its current applications are primarily limited to research settings. As our understanding of its properties and potential expands, it may find broader applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 735270-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,5,2,7 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 735270-31:
(8*7)+(7*3)+(6*5)+(5*2)+(4*7)+(3*0)+(2*3)+(1*1)=152
152 % 10 = 2
So 735270-31-2 is a valid CAS Registry Number.
735270-31-2Relevant academic research and scientific papers
Yenes, Susana,Messeguer, Angel
, p. 14111 - 14122 (1999)
The reactivity of different phenol substrates with nitric oxide and peroxynitrite was investigated. In general, nitration is the major reaction with peroxynitrite, while reactions with aqueous solutions of nitric oxide led to mixtures of nitro and nitroso derivatives depending upon the phenol. Nitrosation occurs on phenol substrates bearing a free para- position with respect to the OH group with the exception of 1-naphthol, which afforded a 1:1 mixture of the 2- and the 4-nitroso derivatives. Chromans 7 and 8 showed the highest reactivity with peroxynitrite, which suggests that they can act as efficient scavengers of this toxic intermediate. In both cases the corresponding 5-nitro derivative was the only reaction product detected. Finally, the fact that chroman 8 reacts with nitric oxide to afford the p- quinone derivative 22a in 90% yield suggests that this antioxidant could also be of potential use as specific nitric oxide tracer in biological tissues.
