← Retour aux articles
Blog Scientifique

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)phenol

Genprice
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)phenol
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)phenolCAS 779331-13-4trifluoromethyl phenol boronic esterpinacol boronateboronic ester building blockorganoboron compoundSuzuki Miyaura coupling reagent

Introduction

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)phenol, CAS 779331-13-4, is an organoboron compound used primarily as a chemical building block for research and organic synthesis.

The compound has the molecular formula C₁₃H₁₆BF₃O₃ and a molecular weight of approximately 288.07 g/mol. Its structure combines a phenolic group, a trifluoromethyl substituent and a cyclic pinacol boronate ester

Produits associés

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

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

JH479230
1 Each
Connectez-vous pour voir le prix

What is CAS 779331-13-4?

CAS 779331-13-4 identifies 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)phenol.


Property
CAS Number779331-13-4
Molecular FormulaC₁₃H₁₆BF₃O₃
Molecular Weight288.07 g/mol
Compound ClassOrganoboron / boronic ester
Typical UseResearch and organic synthesis


These identifiers are consistently reported by chemical databases and commercial chemical suppliers.

Produits associés

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

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

JH479230
1 Each
Connectez-vous pour voir le prix

Why is this boronic ester useful in organic synthesis?

The molecule contains a pinacol boronate (Bpin) group, a functional group widely used in modern synthetic chemistry. Pinacol boronic esters are particularly useful because of their practical stability and their compatibility with carbon-carbon bond-forming transformations.

One important application of organoboron compounds is the Suzuki-Miyaura cross-coupling reaction, in which an organoboron reagent can participate in the construction of new carbon-carbon bonds. This reaction has become an important tool for preparing structurally complex organic molecules.

The presence of both a trifluoromethyl (-CF₃) group and a phenolic hydroxyl group also makes CAS 779331-13-4 an interesting intermediate for the synthesis and diversification of substituted aromatic compounds.

Frequently Asked Questions

What is the CAS number of 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)phenol?

=> The CAS Registry Number is 779331-13-4.

What is its molecular formula?

=> Its molecular formula is C₁₃H₁₆BF₃O₃.

What is its molecular weight?

=> The molecular weight is approximately 288.07 g/mol.

What is it used for?

=> It is mainly relevant as an organoboron research building block and synthetic intermediate. Boronic esters are commonly employed in transformations such as Suzuki-Miyaura cross-coupling.