1256359-10-0

Basic information

• Product Name: 4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER
• Synonyms: 4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER;4,4,5,5-Tetramethyl-2-(4-methyl-2-nitrophenyl)-1,3,2-dioxaborolane
• CAS NO: 1256359-10-0
• Molecular Formula: C13H20BNO5
• Molecular Weight: 281.1126
• Mol File: 1256359-10-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER(1256359-10-0)
• EPA Substance Registry System: 4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER(1256359-10-0)

Safety Data

• Hazardous Substances Data: 1256359-10-0(Hazardous Substances Data)

Usage

General Description

4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER is a chemical compound that belongs to the class of boronic acid pinacol esters. It is a derivative of boronic acid and is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura coupling reaction. This reaction is widely employed in the formation of carbon-carbon bonds, making the compound useful in the production of various pharmaceuticals and agrochemicals. The presence of a nitro group in the molecule provides a unique reactivity, allowing for selective functionalization of the compound in organic reactions. Overall, 4-METHYL-2-NITROPHENYLBORONIC ACID, PINACOL ESTER is a versatile and important chemical in the field of organic chemistry.

Upstream product

• 5326-34-1 4-Bromo-3-nitrotoluene 
• 73183-34-3 bis(pinacol)diborane 

Relevant articles and documents

Preparation method and application of metal organic ternary cyclic compound

The invention belongs to the technical field of fine chemical engineering, and relates to a preparation method and application of a metal organic ternary cyclic compound. In the preparation method, L is used as a ligand, Co2+ in transition metal cobalt salt is used as a node for reaction to prepare the metal organic ternary cyclic compound, and the synthesis route is as follows: L + Co2+ to Co-L; the metal organic ternary cyclic compound prepared by the method disclosed by the invention is novel in idea, good in reduction activity, stable in chemical property and easy for large-scale synthesis, so that the metal organic ternary cyclic compound is easier to put into practical application. The yield of the Co-DPD compound in the reaction of reducing 4-[(4-methoxyphenyl) iminomethyl] methyl benzoate into 4-[(4-methoxyphenyl) aminomethyl] methyl benzoate can reach 83%, and the yields of the Co-DPD compound used for preparing 4-[(4-methoxyphenyl) aminomethyl] benzonitrile and N-(4-methoxyphenyl)-4-(trifluoromethyl)-phenylethylamine can reach 95% and 80% respectively.