1218791-13-9

Basic information

• Product Name: 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester
• Synonyms: 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester;4-(Cbz-Amino)-2-fluorophenylboronic acid, pinacol ester;benzyl (3-fluoro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbaMate;N-[3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamic acid phenylmethyl ester
• CAS NO: 1218791-13-9
• Molecular Formula: C20H23BFNO4
• Molecular Weight: 371.21
• Product Categories: Tedizolid intermediates
• Mol File: 1218791-13-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester(1218791-13-9)
• EPA Substance Registry System: 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester(1218791-13-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 1218791-13-9(Hazardous Substances Data)

Usage

General Description

4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is a chemical compound used in organic synthesis as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. It is commonly used in the Suzuki-Miyaura cross-coupling reaction to introduce the 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid moiety into various organic molecules. 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is also used in the synthesis of pharmaceuticals and agrochemicals, as well as in material science for the creation of functionalized materials and polymers. Additionally, it has been studied for its potential anti-cancer and anti-inflammatory properties. Its unique structure and versatile reactivity make it a valuable tool in the field of organic chemistry.