789-54-8

Basic information

• Product Name: 2,6-di-tert-butyl-4-methylphenoxydichlorophosphine
• Synonyms: 2,6-di-tert-butyl-4-methylphenoxydichlorophosphine
• CAS NO: 789-54-8
• Molecular Weight: 321.227
• Mol File: 789-54-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,6-di-tert-butyl-4-methylphenoxydichlorophosphine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-di-tert-butyl-4-methylphenoxydichlorophosphine(789-54-8)
• EPA Substance Registry System: 2,6-di-tert-butyl-4-methylphenoxydichlorophosphine(789-54-8)

Safety Data

• Hazardous Substances Data: 789-54-8(Hazardous Substances Data)

Upstream product

• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 

Downstream Products

• 128851-18-3 Phosphorous acid 2,6-di-tert-butyl-4-methyl-phenyl ester bis-(2,2,6,6-tetramethyl-piperidin-4-yl) ester 
• 93701-63-4 6-(2,6-Di-tert-butyl-4-methyl-phenoxy)-5,7-dioxa-6-phospha-dibenzo[a,c]cycloheptene 
• 1251852-79-5 C₅₉H₇₇O₅P 
• 135839-87-1 p-tert-butyl-calix[4]arene phosphite 
• 1251852-84-2 25,26;27,28-dibridged p-tert-butyl-calix[4]arene bisphosphite-(C₆H₃(iPr)2-2,6)-(C₆H₂(tBu)-2,6-Me-4) 
• 1251852-82-0 25,26;27,28-dibridged p-tert-butyl-calix[4]arene bisphosphite-(C₆H₃(tBu)2-2,4)-(C₆H₂(tBu)-2,6-Me-4) 
• 107576-85-2 tetracarbonyl(2,6-di-tert-butyl-4-methyl-phenyl-dichlorophosphite)iron 
• 109744-83-4 {Cr(CO)5(PCl₂OC₆H₂-2,6-t-Bu₂-4-Me)} 
• 75895-61-3 O-(2,6-di-tert-butyl-p-tolyl) tetraethylphosphorodiamidothioate 
• 111252-28-9 N-<2,4,6-tri(tert-butyl)phenyl>phosphenimidous acid 2,6-di-tert-butyl-4-methylphenyl ester 

Relevant articles and documents

Monooxychlorophosphine as a novel and efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling of aryl chlorides

A new sterically hindered monooxychlorophosphine was synthesized and the complex generated in situ from its reaction with Pd2(dba)3 promoted the Suzuki-Miyaura reactions of arylboronic acids with aryl chlorides in good yields. Georg Thieme Verlag Stuttgart.

NMR and X-ray crystallographic studies of unsymmetrical 25,26;27,28-dibridged para-tert-butyl calix[4]arene bisphosphites with a large "through-space" P-P coupling

Three 25,26-bridged para-tert-butyl-calix[4]arene phosphites, 1-3, have been synthesized by linking two proximal phenolic oxygen atoms of para-tert-butyl-calix[4]arene to a P(OR) [R = 2,6-But 2-4-Me-C6H2 (1), 2,

Synthese und Reaktivitaet von Phenylethinyl-substituierten Phosphenium-Ion-Komplexen (R)(R')P=MoCp'(CO)2; Darstellung von Clusterverbindungen, die einen 1-Cobalta-2-Phospha-Heteroallyl Synthesebaustein enthalten

The synthesis of the phenylethinyl-chlorophosphines (R)(Cl)P(CC-Ph) (R = 2,6-tBu2-4-MeC6H2O: IVa; R = 2,4,6-tBu3C6H2O: IVb) is described.IV reacts with Cp'(CO)3Mo-, VII, (Cp' = η5-C5H5, ν5-C5Me5) t