922501-02-8 Usage
Description
(4-[4-(DIMETHYLAMINO)BUTYL]PHENYL)BORONIC ACID is a boronic acid derivative with the molecular formula C14H22BNO2. It features a boron atom attached to a phenyl ring and a butyl group with a dimethylamino substituent. This unique structure allows it to participate in a variety of chemical reactions, making it a valuable tool in synthetic chemistry and drug discovery.
Uses
Used in Organic Synthesis:
(4-[4-(DIMETHYLAMINO)BUTYL]PHENYL)BORONIC ACID is used as a building block for the preparation of various functionalized molecules. Its versatile reactivity enables the synthesis of complex organic compounds for a wide range of applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-[4-(DIMETHYLAMINO)BUTYL]PHENYL)BORONIC ACID is used as a key component in the development of pharmaceuticals. Its ability to form stable complexes with metal ions and participate in catalytic reactions makes it a promising candidate for the creation of new drugs.
Used as a Ligand in Transition Metal-Catalyzed Reactions:
(4-[4-(DIMETHYLAMINO)BUTYL]PHENYL)BORONIC ACID is used as a ligand in transition metal-catalyzed reactions. Its coordination with metal ions can enhance the efficiency and selectivity of various catalytic processes, which is crucial for the synthesis of complex organic molecules and pharmaceuticals.
Used as a Potential Inhibitor of Protein Kinases:
Due to its unique structure, (4-[4-(DIMETHYLAMINO)BUTYL]PHENYL)BORONIC ACID has the potential to act as an inhibitor of protein kinases. This makes it a candidate for the development of therapeutic agents targeting kinase-mediated diseases, such as cancer and inflammatory conditions.
Used in Drug Discovery:
The diverse chemical reactivity of (4-[4-(DIMETHYLAMINO)BUTYL]PHENYL)BORONIC ACID makes it a valuable tool in drug discovery. Its ability to participate in various chemical reactions allows researchers to explore its potential in the development of new therapeutic agents and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 922501-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,5,0 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 922501-02:
(8*9)+(7*2)+(6*2)+(5*5)+(4*0)+(3*1)+(2*0)+(1*2)=128
128 % 10 = 8
So 922501-02-8 is a valid CAS Registry Number.
922501-02-8Relevant articles and documents
Oxetanes as promising modules in drug discovery
Wuitschik, Georg,Rogers-Evans, Mark,Mueller, Klaus,Fischer, Holger,Wagner, Bjoern,Schuler, Franz,Polonchuk, Liudmila,Carreira, Erick M.
, p. 7736 - 7739 (2007/10/03)
(Chemical Equation Presented) Ring the changes: Introduction of an oxetane ring results in remarkably improved physico- and biochemical properties of the underlying scaffold. The oxetane ring confers enhanced solubility, reduces the metabolic degredation, lipophilicity, and amphiphilicity, and modulates the basicity of a nearby amine group.
