18232-37-6 Usage
Uses
Used in Organic Synthesis:
2,5-Cyclohexadiene-1,4-dione, O-benzoyloxime oxime is used as a versatile building block for the preparation of various organic compounds. Its unique structure allows for the creation of a wide range of chemical entities, making it an essential component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,5-Cyclohexadiene-1,4-dione, O-benzoyloxime oxime is utilized for the development of pharmaceuticals. Its potential applications in drug discovery are attributed to its ability to be modified and incorporated into various drug candidates, potentially leading to the creation of new therapeutic agents.
Used in Agrochemical Development:
2,5-Cyclohexadiene-1,4-dione, O-benzoyloxime oxime also finds use in the development of agrochemicals. Its chemical properties make it suitable for the synthesis of compounds that can be used in agriculture to protect crops and enhance yields.
Used in Chemical Research:
As a valuable tool for researchers, 2,5-Cyclohexadiene-1,4-dione, O-benzoyloxime oxime is employed in diverse areas of chemistry to study its interesting chemical reactivity. This research can lead to a better understanding of chemical reactions and mechanisms, potentially uncovering new pathways and applications for 2,5-Cyclohexadiene-1,4-dione, O-benzoyloxime oxime.
Check Digit Verification of cas no
The CAS Registry Mumber 18232-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,3 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18232-37:
(7*1)+(6*8)+(5*2)+(4*3)+(3*2)+(2*3)+(1*7)=96
96 % 10 = 6
So 18232-37-6 is a valid CAS Registry Number.
18232-37-6Relevant academic research and scientific papers
Reaction of O-Acyl-1,4-benzoquinone Monooximes with Cyclopentadiene
Avdeenko, A. P.,Glinyanaya, N. M.,Pirozhenko, V. V.
, p. 1066 - 1070 (2007/10/03)
Addition of cyclopentadiene to unsubstituted O-acyl-1,4-benzoquinone monooximes or their 2- or 3-methyl derivatives across the double bond of the quinone ring yielded the only endo-Z isomer, in spite of the possibility for isomerization around the C=N bon
