1321518-06-2

Basic information

• Product Name: 2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
• Synonyms: 2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine;2-Bromo-6-methylpyridine-4-boronic acid, pinacol ester;2-bromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6-methylpyridine
• CAS NO: 1321518-06-2
• Molecular Formula: C12H17BBrNO2
• Molecular Weight: 297.98388
• Mol File: 1321518-06-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(1321518-06-2)
• EPA Substance Registry System: 2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(1321518-06-2)

Safety Data

• Hazardous Substances Data: 1321518-06-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique structure allows for the creation of diverse drug candidates with potential therapeutic applications, leveraging the compound's reactivity in cross-coupling reactions to introduce novel functionalities into drug molecules.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a key building block for the assembly of complex organic molecules. Its ability to participate in Suzuki-Miyaura cross-coupling reactions enables chemists to construct intricate molecular architectures with precision, contributing to the advancement of materials science and the discovery of new chemical entities.
Used in Chemical Research:
2-Bromo-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is utilized as a research tool in academic and industrial laboratories. Its involvement in cross-coupling reactions provides insights into reaction mechanisms, catalyst development, and the exploration of new synthetic methodologies, thereby advancing the frontiers of chemical science.

Relevant articles and documents

1,2,4-TRIAZINE-4-AMINE DERIVATIVES

According to the invention there is provided a compound of formula A1 which may be useful in the treatment of a condition or disorder ameliorated by the inhibition of the A1- A2b or, particularly, the A2a receptor wherein the compound of formula A1 has the structure, wherein, A represents Cy1 or HetA; Cy1 represents a 5- to 14-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one, two or three rings, which Cy1 group is optionally substituted by one or more R4a substituents; HetA represents a 5- to 14-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one, two or three rings and which HetA group is optionally substituted by one or more R4b substituents; B represents a Cy2 or HetB; Cy2 represents a 3- to 10-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one or two rings, which Cy2 group is optionally substituted by one or more R4c substituents; HetB represents a 3- to 10-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one or two rings and which HetB group is optionally substituted by one or more R4d substituents.