1073371-71-7

Basic information

• Product Name: 4-(N-Boc-phenylaminomethyl)benzeneboronic acid pinacol ester
• Synonyms: 4-(N-Boc-phenylaminomethyl)benzeneboronic acid pinacol ester;4-(N-BOC-PHENYLAMINOMETHYL)PHENYLBORONIC ACID PINACOL ESTER;N-BOC-N-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)]BENZYL ANILINE;4-(N-Boc-phenylaminomethyl)phenylboronic acid;[4-(Phenyl-Boc-aminomethyl)phenyl]-boronic acid pinacol ester
• CAS NO: 1073371-71-7
• Molecular Formula: C24H32BNO4
• Molecular Weight: 409.33
• Mol File: 1073371-71-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(N-Boc-phenylaminomethyl)benzeneboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N-Boc-phenylaminomethyl)benzeneboronic acid pinacol ester(1073371-71-7)
• EPA Substance Registry System: 4-(N-Boc-phenylaminomethyl)benzeneboronic acid pinacol ester(1073371-71-7)

Safety Data

• Hazardous Substances Data: 1073371-71-7(Hazardous Substances Data)

Usage

General Description

The chemical 4-(N-Boc-phenylaminomethyl)benzeneboronic acid pinacol ester is a boronic acid derivative that is commonly used in organic synthesis and medicinal chemistry. It contains a boronic acid functional group, making it useful for Suzuki-Miyaura coupling reactions to form carbon-carbon bonds. Additionally, it contains a Boc-protected amine, making it suitable for organic transformations involving amines. The pinacol ester moiety provides stability and protection for the boronic acid group, allowing for selective reactivity in various reactions. Overall, this compound is a versatile building block for the synthesis of complex molecules and pharmaceuticals.