30540-36-4

Usage

Uses

Used in Organometallic Chemistry:
1-Phenyl-3,4-dimethylphosphole is utilized as a ligand in organometallic chemistry for its ability to form stable complexes with metal ions. This application is crucial for the development of new catalysts and materials with tailored properties.
Used in Catalysis:
As a ligand, 1-Phenyl-3,4-dimethylphosphole is employed in catalysis to enhance the efficiency and selectivity of chemical reactions. Its unique electronic and steric properties contribute to the performance of the catalysts in various industrial processes.
Used in Material Development:
1-Phenyl-3,4-dimethylphosphole is used as a component in the development of new materials, leveraging its aromatic nature and phosphorus content to create materials with specific electronic, optical, or magnetic properties.
Used in Pharmaceutical Industry:
1-Phenyl-3,4-dimethylphosphole is used as a building block in the synthesis of pharmaceuticals, contributing to the creation of novel drug candidates with potential therapeutic applications.
Used in Organic Synthesis:
1-Phenyl-3,4-dimethylphosphole serves as a versatile intermediate in organic synthesis, enabling the preparation of a wide range of complex organic molecules for various applications, including agrochemicals, dyes, and other specialty chemicals.

Upstream product

• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 1073-47-8 phenyldibromophosphine 
• 644-97-3 Dichlorophenylphosphine 
• 109-06-8 α-picoline 
• 926-56-7 4-methyl-1,3-pentadiene 
• 76-09-5 2,3-dimethyl-2,3-butane diol 

Downstream Products

• 56569-35-8 4,5-dimethyl-1-oxo-1-phenyl-2-thiophen-3-yl-1,2-dihydro-1λ⁵-phosphinin-2-ol 
• 56569-34-7 oxyde de phenyl-1-(thienyl-2')-2-hydroxy-2-dimethyl-4,5-dihydro-1,2-phosphorine 
• 56569-32-5 2-(4-fluoro-phenyl)-4,5-dimethyl-1-oxo-1-phenyl-1,2-dihydro-1λ⁵-phosphinin-2-ol 
• 41902-15-2 l'oxyde d'hydroxy-2-dimethyl-4,5-diphenyl-1,2-dihydro-1,2-phosphorine 
• 56569-31-4 2-(4-chloro-phenyl)-4,5-dimethyl-1-oxo-1-phenyl-1,2-dihydro-1λ⁵-phosphinin-2-ol 
• 56569-30-3 2-(4-methoxy-phenyl)-4,5-dimethyl-1-oxo-1-phenyl-1,2-dihydro-1λ⁵-phosphinin-2-ol 
• 100-47-0 benzonitrile 
• 126958-87-0 (1S,2S,6S,7R)-2,6,8,9-Tetramethyl-3,10-diphenyl-3,10-diphospha-tricyclo[5.2.1.0^2,6]deca-4,8-diene 3,10-dioxide 
• 90382-81-3 oxyde de phenyl-1-(furyl-2')-2-hydroxy-2-dimethyl-4,5-dihydro-1,2-phosphorine 
• 124747-41-7 2,4,7,9-Tetrabenzhydrylidene-5-phenyl-1,3,6,8-tetraoxa-5λ⁵-phospha-spiro[4.4]nonane 
• 79032-32-9 1,2,6,7-Tetramethyl-8a-phenyl-3,5,8,8a-tetrahydro-phosphindolizine 
• 79032-37-4 3,4-dimethyl-2,5,6-triphenyl-1-phosphanorbornadiene 

Relevant academic research and scientific papers

Novel Phospholium-Type Cationic Surfactants: Synthesis, Aggregation Properties and Antimicrobial Activity

A series of novel phospholium amphiphilic compounds with straight alkyl chains with different numbers of carbon atoms (12, 14, 15, 16, 17, 18) were synthesized. The quaternary phosphorus, phosphonium cation, is incorporated into a five-membered heterocyclic ring. Their physicochemical properties were investigated by measurements of surface tension, conductivity and dynamic light scattering. The critical micelle concentration (cM), the surface tension value at the cM (γcmc), the surface area at the surface saturation per head group (Acmc), the ionization degree of micelle (α), the free energy of micellization (ΔG°mic), and hydrodynamic diameter (dh) were determined. Antimicrobial activity was tested against bacteria and yeast. The structure–activity relationship was determined.

Formal Transition-Metal-Catalyzed Phosphole C-H Activation for the Synthesis of Pentasubstituted Phospholes

Unprecedented formal transition-metal-catalyzed phosphole C-H functionalization is described in this paper. Pentasubstituted phospholes were prepared via the copper-catalyzed reaction of 1,3,4-trisubstituted phosphole with aryl iodides or bromides under distinct conditions. The developed methodology is able to accommodate a wide variety of substituents, including aryl, heteroaryl, and alkenyl.

Synthesis of 3,4-Dimethyl-1-phenylphosphole, 3,4-Dimethyl-1-phenyl-λ5-phosphole 1-Oxide Dimer, and 3,4-Dimethyl-1-phenyl-2,5-dihydro-λ5-phosphole 1-Oxide

The synthesis of 3,4-dimethyl-1-phenylphosphole, 3,4-dimethyl-1-phenyl-λ5-phosphole 1-oxide dimer, and 3,4-dimethyl-1-phenyl-2,5-dihydrophosphole 1-oxide is described.

3,4-dimethyl-2,5,6-tris(p-sulfonatophenyl)-1-phosphanorbornadiene, process for the preparation thereof and process for the hydroformylation of olefinnically unsaturated compounds

The chemical compound 3,4-dimethyl-2,5,6-tris(p-sulfonatophenyl)-1-phosphanorbernadiene, a process for the preparation thereof and a process for the hydroformylation of olefinically unsaturated compounds with the use of catalysts which contain the aforeme