1217501-08-0 Usage
Uses
Used in Organic Synthesis:
4-(1-(Methoxycarbonyl)cyclopropyl)phenylboronic acid is used as a synthetic intermediate for the preparation of various organic compounds. Its ability to form reversible covalent bonds with different biological molecules makes it a valuable asset in the synthesis of complex organic structures.
Used in Research and Laboratory Settings:
This chemical compound is employed as a research tool in the field of organic chemistry, where it aids in the exploration of new synthetic pathways and the development of novel compounds. Its unique properties and reactivity contribute to the advancement of scientific understanding in this area.
Used in Suzuki Coupling Reactions:
4-(1-(Methoxycarbonyl)cyclopropyl)phenylboronic acid is used as a coupling agent in Suzuki coupling reactions, a significant process in organic chemistry for the formation of carbon-carbon bonds. Its boronic acid group plays a crucial role in facilitating these reactions, enabling the creation of new carbon-carbon linkages in organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1217501-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,5,0 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1217501-08:
(9*1)+(8*2)+(7*1)+(6*7)+(5*5)+(4*0)+(3*1)+(2*0)+(1*8)=110
110 % 10 = 0
So 1217501-08-0 is a valid CAS Registry Number.
1217501-08-0Relevant academic research and scientific papers
Efficient cyclopropanation of aryl/heteroaryl acetates and acetonitriles with vinyl diphenyl sulfonium triflate
Zhou, Mingwei,Hu, Yimin,En, Ke,Tan, Xuefei,Shen, Hong C.,Qian, Xuhong
supporting information, p. 1443 - 1445 (2018/03/12)
A convenient method was developed for the cyclopropanation of aryl acetates and aryl acetonitrile using vinyl diphenyl sulfonium triflate salt. The newly developed conditions are simple, mild, and compatible with a wide range of functional groups, without the need to apply an inert atmosphere, or alkali bases.
