129046-56-6 Usage
Uses
Used in Pharmaceutical Synthesis:
2,5-Cyclohexadiene-1,4-dione, 2-cyclohexyl-5-hydroxy(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Organic Chemistry as a Reagent:
In the field of organic chemistry, 2,5-Cyclohexadiene-1,4-dione, 2-cyclohexyl-5-hydroxy(9CI) serves as a versatile reagent. Its ability to participate in various chemical reactions, such as oxidation, reduction, and substitution, makes it a useful tool for researchers and chemists in their quest to create new organic compounds and materials.
Used in Research and Development:
Due to its unique chemical properties, 2,5-Cyclohexadiene-1,4-dione, 2-cyclohexyl-5-hydroxy(9CI) is employed in various research and development projects. It aids scientists in understanding the fundamental principles of organic chemistry and contributes to the advancement of knowledge in this field.
Used in Industrial Applications:
2,5-Cyclohexadiene-1,4-dione, 2-cyclohexyl-5-hydroxy(9CI)'s versatility and reactivity make it suitable for use in various industrial applications. It can be employed in the production of specialty chemicals, fine chemicals, and other chemical products, contributing to the development of innovative and high-quality products in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 129046-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,4 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129046-56:
(8*1)+(7*2)+(6*9)+(5*0)+(4*4)+(3*6)+(2*5)+(1*6)=126
126 % 10 = 6
So 129046-56-6 is a valid CAS Registry Number.
129046-56-6Relevant articles and documents
A divergent and selective synthesis of ortho- and para-quinones from phenols
Huang, Zheng,Kwon, Ohhyeon,Esguerra, Kenneth Virgel N.,Lumb, Jean-Philip
, p. 5871 - 5885 (2015/08/04)
Abstract We describe a divergent synthesis of substituted ortho- and para-quinones by catalytic aerobic oxygenation of phenols. Substituted quinones are omnipresent in chemistry and biology, but their synthesis frequently suffers from low efficiency and poor scope. Our methodology employs a catalytic aerobic di-functionalization of phenols to aryloxy-ortho-quinones. Regioselective substitution with an alcohol provides the alkoxy substituted ortho- or para-quinone, while hydrolysis affords the para-hydroxyquinone. These are mild and selective conditions for the synthesis of diversely substituted quinones from readily available phenol starting materials.
