1073355-06-2

Basic information

• Product Name: 3-(Tetrahydrofurfurylaminocarbonyl)benzeneboronic acid pinacol ester
• Synonyms: 3-(Tetrahydrofurfurylaminocarbonyl)benzeneboronic acid pinacol ester;[3-(TETRAHYDROFURYLAMINO-1-CARBONYL)PHENYL] BORONIC ACID PINACOL ESTER;3-(TETRAHYDROFURFURYLAMINOCARBONYL)PHENYLBORONIC ACID PINACOL ESTER;N-TETRAHYDROFURFURYL-3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZAMIDE;3-(Tetrahydrofurfurylaminocarbonyl)phenylboronic;[3-(Tetrahydrofurfurylamino-1-carbonyl)-phenyl]boronic acid pinacol ester;{3-[(Tetrahydrofuran-2-ylmethyl)carbamoyl]phenyl}boronic acid pinacol ester
• CAS NO: 1073355-06-2
• Molecular Formula: C18H26BNO4
• Molecular Weight: 331.21
• Mol File: 1073355-06-2.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(Tetrahydrofurfurylaminocarbonyl)benzeneboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Tetrahydrofurfurylaminocarbonyl)benzeneboronic acid pinacol ester(1073355-06-2)
• EPA Substance Registry System: 3-(Tetrahydrofurfurylaminocarbonyl)benzeneboronic acid pinacol ester(1073355-06-2)

Safety Data

• Hazardous Substances Data: 1073355-06-2(Hazardous Substances Data)

Usage

General Description

3-(Tetrahydrofurfurylaminocarbonyl)benzeneboronic acid pinacol ester is a complex chemical compound that is often used in the field of organic chemistry. It features a range of distinctive functional groups including boronic acid, ester, and carbonyl. The boronic acid pinacol ester group indicates this compound might be used in Suzuki-Miyaura cross-coupling reactions, which is commonly employed in the synthesis of complex organic molecules. The exact properties and uses of this compound, however, can vary greatly depending on the specifics of its structural arrangement and the context of its application. No specific details about its physical and chemical properties or its usage are provided in common databases.