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Usage

Uses

Used in Organic Synthesis:
Bis(2-cyanoethyl)phenylphosphine is used as a reagent in various organic synthesis processes. Its unique structure allows it to participate in a range of chemical reactions, contributing to the formation of complex organic molecules.
Used in Organometallic Chemistry:
In the field of organometallic chemistry, Bis(2-cyanoethyl)phenylphosphine is employed as a ligand. Ligands are molecules that bind to a central metal atom, forming coordination complexes. The presence of this phosphine in organometallic compounds can influence their stability, reactivity, and overall properties, making it a valuable component in the synthesis of metal complexes.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the potential applications of Bis(2-cyanoethyl)phenylphosphine in the pharmaceutical industry can be inferred. Given its role in organic synthesis and organometallic chemistry, it may be used in the development of new drug molecules or as a component in drug delivery systems, contributing to advancements in medicinal chemistry.
Used in Research and Development:
Bis(2-cyanoethyl)phenylphosphine may also be utilized in research and development settings, where its unique properties can be explored for potential applications in various scientific fields. Researchers may investigate its interactions with other chemicals, its role in catalytic processes, or its potential use in the synthesis of novel materials.

InChI:InChI=1/C12H13N2P/c13-8-4-10-15(11-5-9-14)12-6-2-1-3-7-12/h1-3,6-7H,4-5,10-11H2

Upstream product

• 107-13-1 acrylonitrile 
• 638-21-1 phenylphosphane 
• 15684-35-2 cobalt(II) tetrafluoroborate hexahydrate 
• 4023-53-4 tris(2-cyanoethyl)phosphine 
• 137-26-8 Thiram 

Downstream Products

• 6775-01-5 bis(3-aminopropyl)phenylphosphine 
• 15270-80-1 3,3'-phenylphosphonoyl-di-propionitrile 
• 23848-09-1 4-amino-1-phenyl-1,2,5,6-tetrahydro-phosphinine-3-carbonitrile 
• 6420-84-4 3,3'-phenylphosphonoyl-di-propionic acid 
• 23855-91-6 1-phenyl-1,2,3,6-tetrahydro-phosphinine 
• 23855-92-7 1-benzyl-1-phenyl-1,2,3,6-tetrahydro-phosphininium; bromide 
• 23855-93-8 1-benzyl-3,4-dibromo-1-phenyl-phosphinanium; bromide 
• 23855-87-0 1-phenyl-4-phosphorinanone 
• 64225-48-5 β-Cyanoethyl-2-methoxyethylphenylphosphine 
• 117228-32-7 (η-MeC5H4)Fe{PPh(CH2CH2CN)2}COMe 
• 117227-97-1 (η-Cp)Fe(CO){PPh(CH2CH2CN)2}COMe 
• 101166-33-0 cis-((cyanoethyl)2(Ph)P)2PtCl₂ 
• 214550-15-9 Co(C₄H₇N₂O₂)2(CH₃)(P(CH₂CH₂CN)2(C₆H₅)) 

Relevant academic research and scientific papers

A Commercially Available Ruthenium Compound for Catalytic Hydrophosphination

Hydrophosphination with a commercially available ruthenium compound, bis(cyclopentadienylruthenium dicarbonyl) dimer ([CpRu(CO)2]2), was explored. Styrene derivatives or Michael acceptors react readily with either primary or secondar

Preparation, crystal structures, and behavior in solution of cobalt(III) complexes containing 2-cyanoethylphosphines: Trans-[Co(Me2dtc) 2{P(CH2CH2CN)nPh3-n}] BF4 (n = 1-3; Me

A series of cobalt(III) complexes containing 2-cyanoethylphosphines, [Co(Me2dtc)2{P(CH2CH2CN) nPh3-n}2]BF4{Me2dtc -: N,N-dimethyldithiocarbamate;

Highly effective NPN-type tridentate ligands for asymmetric transfer hydrogenation of ketones

New chiral NPN-type tridentate ligands containing two oxazoline rings and one phosphine have been synthesized, and their Ru(II) complexes show high reactivity and enantioselectivity in transfer hydrogenations of both aryl alkyl and dialkyl ketones (with e

Synthesis and investigation of phosphine ligands containing cationic guanidino functions in aqueous Heck reactions

Phosphines 2 and 3 supplemented with strongly basic and hydrophilic guanidium functions were prepared for the first time. In combination with palladium acetate these ligands form active catalysts that promote an aqueous Heck reaction.