1224738-67-3 Usage
Uses
Used in Pharmaceutical Research and Development:
2H-1-Benzopyran-2-one, 4-(4-fluorophenyl)-3,4-dihydrois used as a chemical intermediate for the synthesis of drug candidates. Its unique structure allows it to interact with specific biological pathways, making it a valuable component in the development of new pharmaceuticals.
Used in Agrochemical Development:
Due to its potential biological activities, 2H-1-Benzopyran-2-one, 4-(4-fluorophenyl)-3,4-dihydromay be utilized in the development of novel agrochemicals. Its ability to target specific biological pathways could contribute to the creation of more effective and targeted pest control solutions.
Used in Industrial Processes:
2H-1-Benzopyran-2-one, 4-(4-fluorophenyl)-3,4-dihydro-'s unique properties may also find applications in various industrial processes. Its potential use in these areas could lead to the development of innovative products and technologies that benefit a range of industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1224738-67-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,7,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1224738-67:
(9*1)+(8*2)+(7*2)+(6*4)+(5*7)+(4*3)+(3*8)+(2*6)+(1*7)=153
153 % 10 = 3
So 1224738-67-3 is a valid CAS Registry Number.
1224738-67-3Relevant academic research and scientific papers
A palladium-catalyzed regioselective hydroesterification of alkenylphenols to lactones with phenyl formate as CO source
Wang, Haining,Dong, Ben,Wang, Yang,Li, Jingfu,Shi, Yian
supporting information, p. 186 - 189 (2014/01/23)
An effective Pd(OAc)2-PPh3 catalyzed hydroesterification of alkenylphenols with phenyl formate as CO surrogate is described. A variety of lactones are obtained in generally high yields with high regioselectivities. In one case, 76% ee is obtained with a chiral ligand.
Rhodium-catalyzed domino conjugate addition-cyclization reactions for the synthesis of a variety of N- and O-heterocycles: Arylboroxines as effective carbon nucleophiles
Park, Ja Ock,Youn, So Won
supporting information; experimental part, p. 2258 - 2261 (2010/07/17)
Facile and efficient Rh(I)-catalyzed domino conjugate addition-cyclization reactions of olefins bearing two electrophilic sites and a pendant nucleophile with organoboroxines have been developed to afford a variety of N- and O-heterocycles, such as 3,4-dihydroquinolin-2(1H)-ones, 3,4-dihydrocoumarins, and pyrrolidin-2-ones, which constitute important motifs in biologically active natural and synthetic organic compounds.
