243990-53-6 Usage
Uses
Used in Organic Synthesis:
4-Benzyloxy-3-methoxybenzeneboronic acid is used as a reagent in Suzuki-Miyaura coupling reactions for forming carbon-carbon bonds. This method is widely employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Benzyloxy-3-methoxybenzeneboronic acid is used as a key intermediate in the synthesis of various biologically active compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 4-Benzyloxy-3-methoxybenzeneboronic acid is utilized for the synthesis of bioactive compounds with pesticidal or herbicidal properties, contributing to the development of more effective and environmentally friendly agrochemicals.
4-Benzyloxy-3-methoxybenzeneboronic acid is a white to off-white powder that is stable under normal temperatures and pressures. It should be stored in a cool, dry place to maintain its stability and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 243990-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,9,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 243990-53:
(8*2)+(7*4)+(6*3)+(5*9)+(4*9)+(3*0)+(2*5)+(1*3)=156
156 % 10 = 6
So 243990-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H15BO4/c1-18-14-9-12(15(16)17)7-8-13(14)19-10-11-5-3-2-4-6-11/h2-9,16-17H,10H2,1H3
243990-53-6Relevant academic research and scientific papers
Total synthesis of quebecol
Cardinal, Sébastien,Voyer, Normand
, p. 5178 - 5180 (2013/09/02)
We report here the total synthesis of quebecol, a new polyphenolic compound with potential applications recently isolated from maple syrup and produced during the condensation of the tree acer saccharum's sap. The synthetic approach we developed involves, as key steps, the formation of a dibromoalkene from an α-ketoester precursor followed by a double Suzuki-Miyaura reaction to unite the three aromatic rings of the target compound on a tetrasubstituted olefin precursor. Our methodology is an efficient pathway to the target compound and leads the way for future analogs.
Synthesis of C-ring hydroxylated neoflavonoids by ligand coupling reactions
Donnelly, Dervilla M.X.,Finet, Jean-Pierre,Guiry, Patrick J.,Rea, Martin D.
, p. 2719 - 2730 (2007/10/03)
Reaction of 4-trifluoromethanesulfonyloxycoumarin derivatives with benzyloxyphenylboronic acid derivatives under modified Suzuki reaction conditions afforded the corresponding neoflavones. Selective debenzylation took place in high yields when the palladi
