106052-22-6

Basic information

• Product Name: Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester
• CAS NO: 106052-22-6
• Molecular Formula: C13H21O4P
• Molecular Weight: 272.281
• Mol File: 106052-22-6.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester(106052-22-6)
• EPA Substance Registry System: Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester(106052-22-6)

Safety Data

• Hazardous Substances Data: 106052-22-6(Hazardous Substances Data)

Upstream product

• 37632-18-1 4-methoxyphenylphosphonic dichloride 
• 67-63-0 isopropyl alcohol 
• 1809-20-7 diisopropyl hydrogenphosphonate 
• 3899-91-0 4-methoxyphenyl p-toluenesulfonate 
• 5720-07-0 4-methoxyphenylboronic acid 
• 3290-99-1 4-methoxybenzoic acid hydrazide 
• 116-17-6 triisopropyl phosphite 
• 104-94-9 4-methoxy-aniline 
• 150-76-5 4-methoxy-phenol 
• 19820-47-4 4-methoxyphenyl 2,2-dimethylpropionate 
• 459-64-3 4-methoxybenzenediazonium tetrafluoroborate 
• 696-62-8 para-iodoanisole 
• 623-12-1 4-chloromethoxybenzene 
• 104-92-7 1-bromo-4-methoxy-benzene 

Relevant articles and documents

Metal-Free Aromatic Carbon-Phosphorus Bond Formation via a Sandmeyer-Type Reaction

An efficient metal-free phosphorylation process based on a Sandmeyer-type transformation with arylamines as the starting materials is developed. The transformation proceeds smoothly at room temperature without the exclusion of moisture or air. This phosphorylation reaction tolerates a wide range of functional groups and affords the phosphorylation products in moderate to good yields, thus providing a valuable method for the formation of aromatic carbon-phosphorus bonds.

Nickel-Catalyzed Phosphorylation of Tosylates

Abstract: Four new bidentate phosphine ligands have been synthesized, characterized and evaluated in Ni-catalyzed C–P coupling reaction. The readily available and inexpensive highly active sulfonate Ni(cod)2-L8 catalyzes the reaction leading to

Aryltrimethylammonium Tetrafluoroborates in Nickel-Catalyzed C–P Bond-Forming Reactions

Abstract: The first nickel-catalyzed phosphorylation of aryltrimethylammonium tetrafluoroborates with the formation of C–P bond instead of C–N has been developed. Starting from easily available and inexpensive aromatic amines, a variety of important arylphosphonates have been synthesized in moderate to excellent yields.