1202245-69-9 Usage
Uses
Used in Organic Chemistry Research:
1-Cyclohexylvinylboronic acid is utilized as a key reagent in Suzuki-Miyaura cross coupling reactions for the formation of carbon-carbon bonds, which is crucial for the synthesis of complex organic molecules and pharmaceutical compounds.
Used in Pharmaceutical Industry:
1-Cyclohexylvinylboronic acid is employed as an intermediate in the development of pharmaceuticals, contributing to the creation of novel drug molecules through its involvement in cross coupling reactions that enhance molecular diversity and complexity.
Used in Material Science:
In the field of material science, 1-Cyclohexylvinylboronic acid is used as a component in the synthesis of advanced materials, such as polymers and composites, where its reactivity in cross coupling reactions allows for the precise construction of desired material properties.
Used in Academic and Industrial Laboratories:
1-Cyclohexylvinylboronic acid is used as a specialized chemical in academic and industrial research settings, where its unique reactivity in cross coupling reactions is harnessed to explore new chemical pathways and develop innovative synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 1202245-69-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,2,4 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1202245-69:
(9*1)+(8*2)+(7*0)+(6*2)+(5*2)+(4*4)+(3*5)+(2*6)+(1*9)=99
99 % 10 = 9
So 1202245-69-9 is a valid CAS Registry Number.
1202245-69-9Relevant academic research and scientific papers
Electrophilic Fluorination of Alkenes via Bora-Wagner–Meerwein Rearrangement. Access to β-Difluoroalkyl Boronates
Biosca, Maria,Himo, Fahmi,Szabó, Kálmán J.,Wang, Qiang
supporting information, p. 26327 - 26331 (2021/11/16)
The electrophilic fluorination of geminal alkyl substituted vinyl-Bmida derivatives proceeds via bora-Wagner–Meerwein rearrangement. According to DFT modelling studies this rearrangement occurs with a low activation barrier via a bora-cyclopropane shaped TS. The Bmida group has a larger migration aptitude than the alkyl moiety in the Wagner–Meerwein rearrangement of the presented electrophilic fluorination reactions.
