762287-58-1 Usage
General Description
2-Fluoro-3-tolylboronic acid is a chemical compound with the formula C7H7BFO2. It is a boronic acid derivative that is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. 2-FLUORO-3-TOLYLBORONIC ACID is characterized by a fluorine atom and a tolyl group attached to the boron atom, making it a versatile and valuable building block in the development of pharmaceuticals, agrochemicals, and materials. 2-Fluoro-3-tolylboronic acid is often used in cross-coupling reactions and other transformations to introduce the 2-fluoro-3-tolyl substituent into various organic molecules. Its unique structure and reactivity make it a valuable tool for the synthesis of a wide range of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 762287-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,2,2,8 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 762287-58:
(8*7)+(7*6)+(6*2)+(5*2)+(4*8)+(3*7)+(2*5)+(1*8)=191
191 % 10 = 1
So 762287-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BFO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4,10-11H,1H3
762287-58-1Relevant articles and documents
General method for the synthesis of substituted phenanthridin-6(5H)-ones using a KOH-mediated anionic ring closure as the key step
Dubost, Emmanuelle,Magnelli, Rosa,Cailly, Thomas,Legay, Rémi,Fabis, Frédéric,Rault, Sylvain
experimental part, p. 5008 - 5016 (2010/08/13)
Substituted phenanthridin-6(5H)-ones were obtained in a two-step procedure involving a Suzuki cross-coupling reaction followed by a KOH-mediated anionic ring closure. The influence of the nature and the position of the substituents on the cyclization step were studied. This methodology offers a general and practical route to diversely substituted phenanthridin-6(5H)-ones.
