172940-58-8 Usage
General Description
2-(N-methyl-N-phenyl)aminomethylbenzeneboronic acid is a chemical compound used in organic synthesis and medicinal chemistry. It is an important building block in the development of pharmaceuticals and biologically active molecules. 2-(N-METHYL-N-PHENYL)AMINOMETHYLBENZENEBORONIC ACID contains a boronic acid functional group, which is commonly used in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds. Additionally, the presence of the amino and phenyl groups make it a versatile building block for creating diverse chemical structures. Its ability to form stable complexes with biological molecules makes it a valuable tool in the development of new drugs and chemical probes for studying biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 172940-58-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 172940-58:
(8*1)+(7*7)+(6*2)+(5*9)+(4*4)+(3*0)+(2*5)+(1*8)=148
148 % 10 = 8
So 172940-58-8 is a valid CAS Registry Number.
172940-58-8Relevant articles and documents
Reactivity of 2-formylphenylboronic acid toward secondary aromatic amines in amination-reduction reactions
Adamczyk-Wo?niak, Agnieszka,Fratila, Raluca M.,Madura, Izabela D.,Pawe?ko, Alicja,Sporzyński, Andrzej,Tumanowicz, Marta,Velders, Aldrik H.,Y?a, Jacek
experimental part, p. 6639 - 6642 (2012/01/14)
The synthesis of 2-(arylaminomethyl)phenylboronic acid via an amination-reduction reaction has been investigated within a model system comprising 2-formylphenylboronic acid and N-ethylaniline. Adoption of the appropriate reaction conditions influences the reactivity of 2-formylphenylboronic acid, enabling efficient synthesis of so-far unobtainable 2-(arylaminomethyl)phenylboronic compounds. The first crystal structure of the aromatic amine derivative has been determined and described.
