18350-98-6

Basic information

• Product Name: Phosphorodichloridic acid, 2,6-dimethylphenyl ester
• CAS NO: 18350-98-6
• Molecular Formula: C8H9Cl2O2P
• Molecular Weight: 239.038
• Mol File: 18350-98-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phosphorodichloridic acid, 2,6-dimethylphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphorodichloridic acid, 2,6-dimethylphenyl ester(18350-98-6)
• EPA Substance Registry System: Phosphorodichloridic acid, 2,6-dimethylphenyl ester(18350-98-6)

Safety Data

• Hazardous Substances Data: 18350-98-6(Hazardous Substances Data)

Upstream product

• 576-26-1 2.6-dimethylphenol 

Downstream Products

• 1334304-33-4 25,26;27,28-dibridged p-H-calix[4]arene bisphosphite-(C₆H₃(Me)2-2,6) 
• 959934-49-7 bis(3-aminophenyl)-2,6-dimethylphenyl phosphate 
• 18350-95-3 Bis(2,6-dimethylphenyl) N-benzylphosphoramidate 
• 21254-87-5 Phosphorsaeure-(2,6-dimethyl-phenylester)-bis-benzylamid 
• 13388-86-8 2,5-dimethylphenyl phosphate 
• 130557-88-9 4-(2,6-Dimethyl-phenoxy)-3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalene 4-oxide 
• 125790-34-3 C₂₀H₁₇Cl₂N₂O₃P 
• 137734-72-6 C₂₉H₂₃O₄P 
• 138650-16-5 2,10-Dichloro-6-(2,6-dimethyl-phenoxy)-12H-5,7-dioxa-6-phospha-dibenzo[a,d]cyclooctene 6-oxide 

Relevant articles and documents

METHOD FOR PRODUCING AN AMINO GROUP-CONTAINING PHOSPHATE COMPOUND, AND A FLAME-RETARDANT RESIN AND FLAME-RETARDANT RESIN COMPOSITION

The present invention relates to a method for producing an amino group-containing phosphate compound, by which the compound can be easily synthesized through a one-step reaction. The method for producing an amino group-containing phosphate compound compri

Syntheses and spectral characterization of 2-aryloxy - 5,5′- bis(bromomethyl)-1,3,2P-dioxaphosphorinane 2-oxides

2-Aryloxy-5,5′-bis(bromomethyl)-1,3,2-dioxaphosphorinane 2-oxides 3 have been synthesized by the reaction of 2,2′-bis(bromomethyl)-1,3- propanediol 1 with various arvlphosphorodichloridates 2a-h in the presence of triethylamine in dry tetrahydrofuran at room temperatuure. Their 1H, 13C, 31P NMR and mass spectral data are discussed.