4-(Trifluoromethyl)phenylboronic acid

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
α,α,α-Trifluoro-p-tolylboronic acid, 4-(Trifluoromethyl)benzeneboronic acid
Trifluoromethylated Buidling Blocks
KUMI3F245
128796-39-4
MFCD00151855
2734389
3544189
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Melting Point
Packaging
Storage
4-(Trifluoromethyl)phenylboronic acid
C7H6BF3O2
189.93
≥99%
White to Off-white Solid
245-250°C
5g,10g,20g,50g,100g,500g,1kg,25kg and 50kg
Store at room temperature
4-(Trifluoromethyl)phenylboronic acid is commonly used as reagent for site-selective suzuki-miyaura cross-coupling reactions. It is also employed as building blocks in the preparation of thiazole derivatives for printable electronics and terphenyl benzimidazoles as tubulin polymerization inhibitors.
 An Efficient Base-Free N-Arylation of Imidazoles and Amines with Arylboronic Acids Using Copper-Exchanged Fluorapatite. [1]
 Efficient synthesis of arylated coumarins by site-selective Suzuki-Miyaura cross-coupling reactions of the bis(triflate) of 4-methyl-5,7-dihydroxycoumarin. [2]
Pd-catalyzed direct arylation of phenylpyrazole: Synthesis of fipronil derivatives with aryl boronic acids promoted by a stoichiometric amount of NIS. [3]
References:
[1] M.Lakshmi Kantam, et al, J. Org. Chem., 2006, 71(25), pp 9522-9524.
[2] N.Eleya, et al, Synlett, 2012, 4(2), pp 223-226.
[3] X.H.Zhang, et al, J. F. Chem., 2012, 137, pp 44-49.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Warning
H302

2931900090
NONH for all modes of transport

1. Product Specification
2. Safety Data Sheet
Please inquire for pricing and availability of this product by writing email to sales@kumidas.com.