73599-99-2 Usage
Uses
Used in Pharmaceutical Industry:
3-methylphenyl tricyclo[3.3.1.1~3,7~]decane-1-carboxylate is utilized as a precursor in the synthesis of various drugs and organic compounds. Its specific molecular structure and functional groups contribute to the development of new pharmaceutical agents, enhancing the range of therapeutic options available.
Used in Chemical Industry:
In the chemical industry, 3-methylphenyl tricyclo[3.3.1.1~3,7~]decane-1-carboxylate serves as a key intermediate for the production of a variety of organic compounds. Its unique structure allows for the creation of complex molecules that can be used in different chemical processes and products.
Used in Materials Science:
3-methylphenyl tricyclo[3.3.1.1~3,7~]decane-1-carboxylate may have potential applications in materials science due to its specific structure and properties. Its use could lead to the development of new materials with unique characteristics, contributing to advancements in this field.
Used in Medicinal Chemistry:
3-methylphenyl tricyclo[3.3.1.1~3,7~]decane-1-carboxylate also holds promise in medicinal chemistry, where its structure and properties can be leveraged to design and synthesize new pharmaceutical agents with improved efficacy and selectivity. This makes it a valuable tool for the development of innovative treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 73599-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,9 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73599-99:
(7*7)+(6*3)+(5*5)+(4*9)+(3*9)+(2*9)+(1*9)=182
182 % 10 = 2
So 73599-99-2 is a valid CAS Registry Number.
73599-99-2Relevant articles and documents
Pd(II)-catalyzed C-H activation/aryl-aryl coupling of phenol esters
Xiao, Bin,Fu, Yao,Xu, Jun,Gong, Tian-Jun,Dai, Jian-Jun,Yi, Jun,Liu, Lei
supporting information; experimental part, p. 468 - 469 (2010/03/25)
(Chemical Equation Presented) Although nitrogen-containing group-directed cyclopalladation reactions have been well-known, Pd(II) insertion into C-H bonds promoted by coordination of an oxygen-only group to the palladium remains rather rare. In the present study, the first cyclopalladation complex formed from a simple phenol ester was characterized by X-ray crystallography. A promising protocol for the ortho C-H activation/aryl-aryl coupling of phenol esters that was not sensitive to moisture or air was then established. The utility of the reaction was demonstrated for the synthesis of useful phenol derivatives. Copyright
