248274-03-5 Usage
Uses
Used in Organic Synthesis:
2-(Aminomethyl)phenyl boronic acid is used as a building block in organic synthesis for the preparation of various biologically active compounds and pharmaceuticals. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties.
Used in Material Science:
In the field of material science, 2-(Aminomethyl)phenyl boronic acid is utilized in the development of novel materials for electronic and optical applications. Its chemical properties enable the design of advanced materials with improved performance characteristics.
Used in Catalysis:
2-(Aminomethyl)phenyl boronic acid also finds application in the field of catalysis, where it can act as a catalyst or a catalyst precursor in various chemical reactions. Its ability to form stable complexes with other molecules makes it a valuable component in catalytic processes.
Used in Pharmaceutical Industry:
2-(Aminomethyl)phenyl boronic acid has been investigated for its potential as a therapeutic agent for the treatment of cancer and other diseases. Its unique structure allows for the development of targeted drug delivery systems and the modulation of biological pathways, offering new avenues for disease treatment and management.
Check Digit Verification of cas no
The CAS Registry Mumber 248274-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,8,2,7 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 248274-03:
(8*2)+(7*4)+(6*8)+(5*2)+(4*7)+(3*4)+(2*0)+(1*3)=145
145 % 10 = 5
So 248274-03-5 is a valid CAS Registry Number.
248274-03-5Relevant articles and documents
BROMODOMAIN LIGANDS CAPABLE OF DIMERIZING IN AN AQUEOUS SOLUTION
-
Paragraph 00497; 00498, (2015/06/11)
Described herein are monomers capable of forming a biologically useful multimer when in contact with one, two, three or more other monomers in an aqueous media. In one aspect, such monomers may be capable of binding to another monomer in an aqueous media (e.g. in vivo) to form a multimer (e.g. a dimer). Contemplated monomers may include a ligand moiety, a linker element, and a connector element that joins the ligand moiety and the linker element. In an aqueous media, such contemplated monomers may join together via each linker element and may thus be capable of modulating one or more biomolecules substantially simultaneously, e.g., modulate two or more binding domains on a protein or on different proteins.
Small molecule thienopyrimidine-based protein tyrosine kinase inhibitors
-
Page/Page column 40, (2010/02/15)
Various thienopyrimidine-based analog compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.
