4073-31-8

Basic information

• Product Name: (diethylamino)phenylchlorophosphine
• Synonyms: (diethylamino)phenylchlorophosphine
• CAS NO: 4073-31-8
• Molecular Weight: 215.663
• Mol File: 4073-31-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: (diethylamino)phenylchlorophosphine(CAS DataBase Reference)
• NIST Chemistry Reference: (diethylamino)phenylchlorophosphine(4073-31-8)
• EPA Substance Registry System: (diethylamino)phenylchlorophosphine(4073-31-8)

Safety Data

• Hazardous Substances Data: 4073-31-8(Hazardous Substances Data)

Upstream product

• 644-97-3 Dichlorophenylphosphine 
• 1636-14-2 bis(diethylamino)phenylphosphine 
• 109-89-7 diethylamine 

Downstream Products

• 146286-07-9 Phenyl-phenylethinyl-phosphinigsaeure-diethylamid 
• 188608-10-8 [3-(N,N-bis(trimethylsilyl)amino)phenyl](diethylamino)phenylphosphine 
• 101078-12-0 (CO)5W{PhP(NEt₂)(CHCH₂)} 
• 92573-07-4 (2-methoxyphenyl)(phenyl)phosphine chloride 
• 1359677-32-9 C₄H₉C₆H₄SO₂NPH(C₆H₅)C₆H₄OCH₃ 
• 1158247-92-7 C₂₃H₂₆NO₃PS 
• 1254976-86-7 C₄₀H₅₄P₂S₂Si₂ 

Relevant articles and documents

Synthesis and structure of bis-phosphorylated 1,4:3,6-dianhydro-D-mannitol derivatives

A number of bis-phosphorylated 1,4:3,6-dianhydro-D-mannitol derivatives were synthesized. The increased steric loading of the phosphorus-containing residues in the compounds prepared gives rise to complicated 1H and 31P NMR spectra a

New Access to Six-Membered Phosphacycle Annulated Polyaromatic Ring System

A facile Ag-catalyzed intramolecular C–P bond formation reaction from easily accessible phosphine oxides has been developed. Several new heteroatoms fused π-conjugated molecules were synthesized from this procedure with their structures confirmed by X-ray

Polyhedral oligomeric silsesquioxane-conjugated bis(diphenylphosphino)amine ligand for chromium(III) catalyzed ethylene trimerization and tetramerization

Polyhedral oligomeric silsesquioxanes (POSSs) were attached to conventional bis(diphenylphosphino)amine (PNP) ligand as solubility-enhancing materials for catalytic ethylene trimerization and tetramerization. Differently functionalized arylphosphine ligands of the type (Ph)2PN(POSS)P(Ph)(ArR) (R = functional groups) were systematically developed, and their corresponding chromium(III) complexes were formed. The developed precatalysts exhibited excellent tolerance in solvents, including even low-carbon-number hydrocarbons such as n-pentane, n-hexane, or cyclohexane. In particular, the ortho-fluorophenyl-substituted complex showed higher stability even at higher temperatures above 120 °C. The ortho-OCF3-phenyl-substituted complex showed outstanding catalytic activity, which reached 2287 kg/g Cr/h at 30 bar.