92862-65-2 Usage
Description
1-(2-methoxyphenyl)cycloheptene, with the chemical formula C15H18O, is a cyclic organic compound characterized by a seven-membered ring and a methoxyphenyl group attached to one of the carbons in the ring. 1-(2-methoxyphenyl)cycloheptene is recognized for its unique structural features and chemical properties, making it a valuable asset in the fields of organic synthesis and pharmaceutical research. Its potential applications in the development of new drugs and materials render it a subject of interest for researchers across various scientific disciplines.
Uses
Used in Organic Synthesis:
1-(2-methoxyphenyl)cycloheptene is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse properties and potential applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-methoxyphenyl)cycloheptene serves as a valuable compound for drug development. Its structural features and chemical properties make it a promising candidate for the design and synthesis of novel therapeutic agents.
Used in Material Science:
1-(2-methoxyphenyl)cycloheptene's unique properties also make it a candidate for the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity, which can be applied in various industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 92862-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,6 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92862-65:
(7*9)+(6*2)+(5*8)+(4*6)+(3*2)+(2*6)+(1*5)=162
162 % 10 = 2
So 92862-65-2 is a valid CAS Registry Number.
92862-65-2Relevant articles and documents
Achieving vinylic selectivity in Mizoroki-heck reaction of cyclic olefins
Wu, Xiaojin,Lu, Yunpeng,Hirao, Hajime,Zhou, Jianrong
supporting information, p. 6014 - 6020 (2013/06/26)
In Heck reactions of cyclic olefins, the products usually have aryl groups that end up at the allylic and/or homoallylic position. We herein report new selectivity that adds aryl groups to the vinylic position. Cyclic olefins of various ring size worked well. The desired isomers were produced by palladium-hydride-catalyzed isomerization of the initial products. Thus, a specific catalyst must be used so that it can perform two jobs under one set of reaction conditions. Copyright
