1049663-21-9 Usage
Boronic acid derivative
2-((N,N-di-n-octyl)aminomethyl)phenylboronic acid is a compound that has a boron atom bonded to a phenyl group and a di-n-octylamine group.
Structure
It consists of a phenylboronic acid core attached to a di-n-octylamine group.
Use as a reagent
It is often used in organic synthesis, particularly in the formation of carbon-carbon and carbon-nitrogen bonds.
Suzuki-Miyaura cross-coupling reaction
It is commonly employed in the Suzuki-Miyaura cross-coupling reaction, which is a method for the coupling of an aryl halide with an organoboron compound to form a biaryl product.
Potential applications
2-((N,N-di-n-octyl)aminomethyl)phenylboronic acid has potential applications in the development of materials for organic electronic devices, such as organic light-emitting diodes and organic photovoltaics.
Check Digit Verification of cas no
The CAS Registry Mumber 1049663-21-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,6,6 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1049663-21:
(9*1)+(8*0)+(7*4)+(6*9)+(5*6)+(4*6)+(3*3)+(2*2)+(1*1)=159
159 % 10 = 9
So 1049663-21-9 is a valid CAS Registry Number.
1049663-21-9Relevant articles and documents
Enhanced fructose, glucose and lactose transport promoted by a lipophilic 2-(aminomethyl)-phenylboronic acid
Duggan, Peter J.,Houston, Todd A.,Kiefel, Milton J.,Levonis, Stephan M.,Smith, Bradley D.,Szydzik, Melanie L.
, p. 7122 - 7126 (2008)
A lipophilic 2-(aminomethyl)-phenylboronic acid (1a) was prepared and used to transport saccharides across a thin supported liquid membrane. The result was the highest recorded fructose flux promoted by a monoboronic acid under near-neutral conditions, and one of the highest fructose/glucose transport selectivities (12.9). The application of a pH gradient across the membrane further enhanced carrier-mediated fructose flux but fructose/glucose selectivity was decreased. The first effective transport of a disaccharide, lactose, was achieved using supported liquid membranes containing a high concentration of 1a (250 mM). A strong carrier concentration effect on lactose transport and a battery of mass spectrometry evidence point to the involvement of 2:1 boronate/lactose esters in this transport process.
