198976-40-8 Usage
Description
[1-(4-FLUORO-PHENYL)-CYCLOPROPYL]-METHANOL is a chemical compound characterized by its molecular formula C10H11FO. It is a cyclopropyl derivative of methanol, featuring a fluorophenyl group attached to the cyclopropyl ring. [1-(4-FLUORO-PHENYL)-CYCLOPROPYL]-METHANOL is known for its unique structural features, which make it a versatile and valuable intermediate in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
[1-(4-FLUORO-PHENYL)-CYCLOPROPYL]-METHANOL is used as a building block for the synthesis of various pharmacologically active compounds. Its cyclopropyl and fluorophenyl moieties contribute to its versatility, making it a valuable component in the development of new drugs and chemical products.
Used in Chemical Industry:
In the chemical industry, [1-(4-FLUORO-PHENYL)-CYCLOPROPYL]-METHANOL serves as an intermediate for creating a range of chemical products. Its unique structural features allow for the synthesis of diverse compounds with potential applications in various fields.
Used in Medicinal Chemistry and Drug Discovery Research:
Due to its unique structural features, [1-(4-FLUORO-PHENYL)-CYCLOPROPYL]-METHANOL may have potential applications in medicinal chemistry and drug discovery research. Researchers can leverage its cyclopropyl and fluorophenyl moieties to design and develop novel compounds with specific therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 198976-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,9,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 198976-40:
(8*1)+(7*9)+(6*8)+(5*9)+(4*7)+(3*6)+(2*4)+(1*0)=218
218 % 10 = 8
So 198976-40-8 is a valid CAS Registry Number.
198976-40-8Relevant articles and documents
Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C?H Bonds
Lee, Taegyo,Hartwig, John F.
supporting information, p. 8723 - 8727 (2016/07/21)
Hydrosilyl ethers, generated in situ by the dehydrogenative silylation of cyclopropylmethanols with diethylsilane, undergo asymmetric, intramolecular silylation of cyclopropyl C?H bonds in high yields and with high enantiomeric excesses in the presence of
