1151564-17-8

Basic information

• Product Name: 2-Chloro-3-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenol
• Synonyms: 2-Chloro-3-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenol;Phenol, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
• CAS NO: 1151564-17-8
• Molecular Formula: C₁₂H₁₆BClO₃
• Molecular Weight: 254.51764
• Mol File: 1151564-17-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Chloro-3-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-3-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenol(1151564-17-8)
• EPA Substance Registry System: 2-Chloro-3-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenol(1151564-17-8)

Safety Data

• Hazardous Substances Data: 1151564-17-8(Hazardous Substances Data)

Usage

Uses

2-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Upstream product

• 214360-76-6 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol 
• 863870-87-5 3 -bromo-2-chlorophenol 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 1151564-03-2 (2-chloro-3-methoxyphenyl)boronic acid pinacol ester 

Relevant articles and documents

PD-L1 ANTAGONIST COMPOUND

Provided is a compound represented by formula (I) and a pharmaceutical composition thereof, as well as a method for using a compound represented by formula (I) to prevent and/or treat immune-related disorders.

Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications

An ortho-selective ammonium chloride salt-catalyzed direct C-H monohalogenation of phenols and 1,1′-bi-2-naphthol (BINOL) with 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) as the chlorinating agent has been developed. The catalyst loading was low (down to 0.01 mol %) and the reaction conditions were very mild. A wide range of substrates including BINOLs were compatible with this catalytic protocol. Chlorinated BINOLs are useful synthons for the synthesis of a wide range of unsymmetrical 3-aryl BINOLs that are not easily accessible. In addition, the same catalytic system can facilitate the ortho-selective selenylation of phenols.