1599432-41-3 Usage
Organoboron compound
A compound containing a boron atom bonded to carbon atoms.
Dioxaborolane ring
A five-membered ring structure consisting of two oxygen atoms and three boron atoms.
Fluoro-methoxyphenyl group
A phenyl group (a six-membered aromatic ring) with a fluorine atom at position 2 and a methoxy group (-OCH3) at position 6.
Chemical synthesis
The process of creating new chemical compounds through chemical reactions.
Pharmaceutical research
The study of new drugs and medications to treat diseases and medical conditions.
Potential application in organic reactions
The possible use of the compound in chemical reactions involving organic molecules.
Suzuki coupling
A type of organic reaction used to form carbon-carbon bonds between two organic molecules.
Building block
A simple molecule that can be used to create more complex molecules through chemical reactions.
Biologically active molecules
Molecules that have an effect on biological processes and can be used as potential drugs or medications.
Development of new pharmaceuticals
The process of creating new drugs and medications to treat diseases and medical conditions.
Unique chemical structure and properties
The compound has a one-of-a-kind structure and properties that make it useful in the field of organic chemistry.
Valuable tool in organic chemistry
The compound's unique structure and properties make it a useful tool for creating new molecules and materials in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1599432-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,9,4,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1599432-41:
(9*1)+(8*5)+(7*9)+(6*9)+(5*4)+(4*3)+(3*2)+(2*4)+(1*1)=213
213 % 10 = 3
So 1599432-41-3 is a valid CAS Registry Number.
1599432-41-3Relevant academic research and scientific papers
Transition metal-free synthesis of pinacol arylboronate: Regioselective boronation of 1,3-disubstituted benzenes
Wang, Yan,Wang, Le,Chen, Ling-Yan,Bhadury, Pinaki S.,Sun, Zhihua
, p. 675 - 678 (2014/05/06)
The regioselective synthesis of pinacol arylboronate has been achieved from 1,3-disubstituted benzene through directed ortho-metallation (DoM)-borylation sequence. A wide range of substituents and borylating reagents were investigated. In situ lithiation and subsequent boronation predominantly occurred at the ortho-position to afford the desired products in moderate yields. CSIRO 2014.
