372193-54-9

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(2-(Prop-1-en-2-yl)phenyl)boronic acid is used as a building block for the production of various pharmaceuticals and agrochemicals. Its versatile reactivity and stability make it a valuable tool for the synthesis of complex organic compounds with potential therapeutic and pesticidal properties.
Used in Organic Synthesis:
(2-(Prop-1-en-2-yl)phenyl)boronic acid is used as a reagent to form carbon-carbon and carbon-heteroatom bonds. Its unique chemical properties and ability to participate in various coupling reactions make it a valuable tool for the preparation of diverse organic compounds.
Used in Drug Development:
(2-(Prop-1-en-2-yl)phenyl)boronic acid has displayed promising potential in the development of new drugs and materials due to its unique chemical properties and ability to participate in various coupling reactions. It can be used as a starting material or intermediate in the synthesis of novel drug candidates with potential therapeutic applications.

Upstream product

• 7073-70-3 1-bromo-2-isopropenylbenzene 
• 688-74-4 boric acid tributyl ester 
• 19647-26-8 (Z)-β-bromo-α-methylstyrene 
• 121-43-7 Trimethyl borate 
• 7732-18-5 water 
• 5419-55-6 Triisopropyl borate 

Downstream Products

• 221352-10-9 3,3-dimethylbenzo [c][1,2]oxaborol-1(3H)-ol 

Relevant academic research and scientific papers

Asymmetric Alkenylation of Enones and Imines Enabled by A Highly Efficient Aryl to Vinyl 1,4-Rhodium Migration

The asymmetric rhodium-catalyzed alkenylation of enones and imines with arylboronic acids has been developed. A highly controllable aryl to vinyl 1,4-rhodium migration is the key step. Stereodefined vinyl moieties were installed in excellent enantioselectivies for most examined examples. DFT calculations reveal that the driving force of this rhodium migration is a kinetically favored process.

Synthesis of substituted benzooxaborinin-1-ols via palladium-catalysed cyclisation of alkenyl- and alkynyl-boronic acids

Two new palladium-catalysed reactions have been developed for the synthesis of stable 4-substituted benzooxaborinin-1-ols. A palladium-catalysed cyclisation of ortho-alkenylbenzene boronic acids can be used to access 4-chlorobenzooxaborinin-1-ols via a Wa

NOVEL POLYMERIZABLE MONOMER, AND MATERIAL FOR ORGANIC DEVICE, HOLE INJECTION/TRANSPORT MATERIAL, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT AND ORGANIC ELECTROLUMINESCENT ELEMENT EACH COMPRISING POLYMER (POLYMERIC COMPOUND) OF THE POLYMERIZABLE MONOMER

A polymerizable monomer represented by the following formula (1) wherein at least one of Ar1 to Ar3 is substituted by a group represented by the following formula (2) and which is substituted by one or more groups comprising a polymerizable functional group. Ar1 to Ar3 are a substituted or unsubstituted aryl group having 6 to 40 ring carbon atoms, Ar6 is a substituted or unsubstituted aryl group having 6 to 40 ring carbon atoms and Ar4 and Ar5 are a substituted or unsubstituted arylene group having 6 to 40 ring carbon atoms.

Bromo-boronolactonization of olefins

Exposure of a variety of mono- and disubstituted ortho-alkenylarylboronic acids to NBS in THF/H2O under neutral conditions affords bromo-boronolactones, in some instances, with exceptional regiocontrol. The adducts, analogous to those formed by carboxylic acids, are shown to be useful synthetic intermediates.