CAS 1015242-08-6: 2-Piperidinopyrimidine-5-boronic acid pinacol ester

Description: 2-Piperidinopyrimidine-5-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is significant in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a piperidine ring, contributing to its basicity and potential interactions with biological targets. The pyrimidine moiety provides additional aromatic character and can participate in hydrogen bonding, influencing its solubility and reactivity. The pinacol ester group enhances the stability of the boronic acid, making it more suitable for storage and handling. Typically, compounds like this are utilized in medicinal chemistry and materials science due to their ability to form covalent bonds with various substrates. The presence of both nitrogen and boron atoms in its structure allows for diverse reactivity patterns, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Overall, this compound exemplifies the intersection of organic chemistry and medicinal applications, showcasing the importance of boronic acids in contemporary chemical research.

Formula: C₁₅H₂₄BN₃O₂

Synonyms:

• 2-(Piperidin-1-yl)pyrimidine-5-boronic acid pinacol ester

Pyrimidine, 2-(1-piperidinyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

CAS: 1015242-08-6

• Formula: C₁₅H₂₄BN₃O₂
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 289.1810

[2-(Piperidin-1-yl)pyrimidin-5-yl]boronic acid, pinacol ester

CAS: 1015242-08-6

• Molecular weight: 289.18g/mol

2-(Piperidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine

CAS: 1015242-08-6

• Purity: 96%
• Molecular weight: 289.19000244140625

2-Piperidin-1-yl-pyrimidine-5-boronic acid pinacol ester

CAS: 1015242-08-6

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• Formula: C₆H₁₂N₂O₃·HCl
• Purity: Min. 95%
• Molecular weight: 196.63 g/mol