1160561-31-8

Basic information

• Product Name: 3-CHLORO-5-(TRIFLUOROMETHYL)BENZENEBORONIC ACID
• Synonyms: 3-CHLORO-5-(TRIFLUOROMETHYL)BENZENEBORONIC ACID;3-Borono-5-chlorobenzotrifluoride
• CAS NO: 1160561-31-8
• Molecular Formula: C7H5BClF3O2
• Molecular Weight: 224.3726096
• Mol File: 1160561-31-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 3-CHLORO-5-(TRIFLUOROMETHYL)BENZENEBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-5-(TRIFLUOROMETHYL)BENZENEBORONIC ACID(1160561-31-8)
• EPA Substance Registry System: 3-CHLORO-5-(TRIFLUOROMETHYL)BENZENEBORONIC ACID(1160561-31-8)

Safety Data

• Statements: 22-36/37/38
• Safety Statements: 36/37/39
• Hazardous Substances Data: 1160561-31-8(Hazardous Substances Data)

Usage

Chemical Properties

White solid

Upstream product

• 98-15-7 3-chlorotrifluoromethylbenzene 
• 942069-65-0 3-chloro-5-methoxybenzene-1-boronic acid pinacol ester 

Relevant articles and documents

One-pot synthesis of arylboronic acids and aryl trifluoroborates by Ir-catalyzed borylation of arenes

(Chemical Equation Presented) The synthesis of arylboronic acids and aryl trifluoroborates in a one-pot sequence by Ir-calalyzed borylation of arenes is reported. To prepare the arylboronic acids, the Ir-catalyzed borylation is followed by oxidative cleavage of the boronic ester with NaIO4. To prepare the aryltrifluoroborate, the Ir-catalyzed borylation is followed by displacement of pinacol by KHF2. These two-step sequences give products that are more reactive toward subsequent chemistry than the initially formed pinacol boronates.