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

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

Uses

Used in Organic Synthesis:
4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds, facilitating the synthesis of complex organic molecules.
Used in the Suzuki-Miyaura Cross-Coupling Reaction:
In the Suzuki-Miyaura cross-coupling reaction, 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is used to introduce the desired 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid moiety into various organic molecules, enabling the creation of a wide range of compounds.
Used in Pharmaceutical Synthesis:
4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is used in the synthesis of agrochemicals, aiding in the development of effective pesticides and other agricultural products.
Used in Material Science:
4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester is used in material science for the creation of functionalized materials and polymers, enhancing their properties and expanding their applications.
Used in Cancer Research:
4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester has been studied for its potential anti-cancer properties, with ongoing research exploring its ability to target and inhibit cancer cell growth.
Used in Inflammation Research:
Additionally, 4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester has been investigated for its potential anti-inflammatory properties, with research focusing on its ability to modulate inflammatory responses and alleviate related conditions.