81639-99-8

Usage

InChI:InChI=1/C16H18ClO3P/c1-11-7-5-8-12(2)15(11)19-21(17,18)20-16-13(3)9-6-10-14(16)4/h5-10H,1-4H3

Upstream product

• 576-26-1 2.6-dimethylphenol 

Downstream Products

• 113088-99-6 Morpholin-4-yl-phosphonic acid bis-(2,6-dimethyl-phenyl) ester 
• 113089-04-6 N,N'-bis[di-(2,6-xylenoxy)phosphinyl]piperazine 
• 139301-35-2 (S)-3-[Bis-(2,6-dimethyl-phenoxy)-phosphoryloxy]-2-tert-butoxycarbonylamino-propionic acid benzyl ester 
• 113089-00-2 Cyclohexyl-phosphoramidic acid bis-(2,6-dimethyl-phenyl) ester 
• 18350-99-7 Bis(2,6-dimethylphenyl) hydrogen phosphate 
• 116992-78-0 Phosphoramidic acid bis-(2,6-dimethyl-phenyl) ester 
• 113947-71-0 bis(2,6-dimethylphenyl) 1-methylene-2-propenyl phosphate 
• 113089-02-4 {2-[Bis-(2,6-dimethyl-phenoxy)-phosphorylamino]-ethyl}-phosphoramidic acid bis-(2,6-dimethyl-phenyl) ester 
• 113089-01-3 anilinodi(2,6-xylenyl)phosphate 
• 18350-95-3 Bis(2,6-dimethylphenyl) N-benzylphosphoramidate 
• 113089-05-7 {4-[Bis-(2,6-dimethyl-phenoxy)-phosphorylamino]-phenyl}-phosphoramidic acid bis-(2,6-dimethyl-phenyl) ester 
• 113089-03-5 (2-{[Bis-(2,6-dimethyl-phenoxy)-phosphoryl]-methyl-amino}-ethyl)-methyl-phosphoramidic acid bis-(2,6-dimethyl-phenyl) ester 
• 869058-03-7 phosphoric acid bis-(2,6-dimethyl-phenyl) ester vinyl ester 
• 116992-89-3 C₁₆H₁₈Cl₃NO₃P₂ 

Relevant academic research and scientific papers

REACTIVE TYPE PHOSPHATE AND PREPARATION PROCESS

Provided herein are phosphorus-based flame retardant compounds that provide both good electrical characteristics and good heat resistance characteristics when incorporated into PCB compositions. In particular, provided herein are new organophosphorus-base

Lubricating oil composition for internal combustion engine

Provided is a lubricating oil composition for an internal combustion engine, including as essential components the following component (A), component (B), and component (C), in which a phosphorus content of the composition is 50 ppm by mass to 1,000 ppm by mass: Component (A): a base oil; Component (B): a compound represented by the following general formula (1); and Component (C): a metal-containing antioxidant: where R1 to R8 each independently represent a hydrogen atom or an alkyl group having 1 to 20 carbon atoms, Z represents a hydrocarbon group having 2 to 20 carbon atoms, and n represents a number of 1 to 10.

Lubricating oil composition

Provided is a lubricating oil composition, including a base oil and a specific condensed phosphate blended with various additives.

Neodymium tris-diarylphosphates: Systematic study of the structure-reactivity relationship in butadiene and isoprene polymerisation

The catalytic properties of neodymium tris-phosphates with various diarylphosphate ligands in the stereoregular 1,4-cis-polymerisation of butadiene and isoprene were studied. The considerable variability of the diaryl phosphate structure allowed for the systematic investigation of the dependence of the catalytic properties of neodymium tris-diarylphosphates on the electronic and steric properties of the ligand. Electron-withdrawing substituents (F, Cl, Br) in the aryl moiety increased the catalyst activity of tris-diarylphosphate. Neodymium aryl phosphates containing lipophilic bulky ligands provided the synthesis of polydienes with a monomodal molecular-weight distribution. The optimal catalytic properties demonstrated that the neodymium aryl phosphate prepared from bis(2,6-dimethyl-4-tert-butylphenyl)-phosphoric acid showed high activity and ensured a monomodal MWD of polydienes (Mw/Mn ～ 2 for polybutadiene and Mw/Mn ～ 3 for polyisoprene) in various conditions.

METHOD FOR PRODUCING AROMATIC DIPHOSPHATES

A method for producing an aromatic diphosphate comprising: Step 1 which is a step where a specific aromatic monohydroxy compound having a steric hindrance group at ortho-positions is made to react with phosphorus oxyhalide in the presence of a Lewis acid

Artemisinin-derived dimer phosphate esters as potent anti-cytomegalovirus (anti-CMV) and anti-cancer agents: A structure-activity study

We recently reported the anti-cancer and anti-cytomegalovirus (CMV) activity of artemisinin-derived trioxane diphenylphosphate dimer 838. To probe the relationship between chemical structure and anti-CMV and anti-cancer activities, we now report synthesis and evaluation of a series of eight new dimer phosphate ester analogs of 838. This series of novel molecules was screened against human foreskin fibroblasts (HFFs) infected with CMV and against the human Jurkat T cell acute lymphoblastic leukemia cell line. This SAR study confirms the very high anti-CMV and anti-cancer potencies of dimer diphenyl phosphate ester 838 without its being toxic to normal cells.

PHOSPHORUS FLAME RETARDANT, FLAME-RETARDANT RESIN COMPOSITION CONTAINING SAME, AND MOLDED BODY

A phosphorus flame-retardant composition characterized in that it comprises an aromatic diphosphate compound represented by the general formula (I): wherein R1 and R2 are, the same or different, a lower alkyl group, R3 and

Crystalline powders of aromatic diphosphates, their preparation and use

Crystalline powders of an aromatic diphosphate of the formula (I): wherein R1 and R2 are, the same or different, a lower alkyl group, R3 is a hydrogen atom or a lower alkyl group, R4 is a hydrogen atom or a lower alkyl group, Y is a bonding arm, -CH2-, -C(CH3)2-, -S-, -SO2-, -CO-, -O- or -N=N-, k is 0 or 1 and m is an integer of 0 to 4.

STABILE ADDUKTE BEI DER CHLORIERUNG VON 2,6-DIMETHYLPHENYLPHOSPHITEN

PIII compounds of type 4 react with chlorine to give stable adducts.The phosphite 4a gives the chlorophosphonium chloride 6 and the chlorophosphites 4b and 4c give the chlorophosphoranes 8 and 10.Key words: Chlorophosphonium salts; trichloro-di

Improved protective groups for phosphate of o-phosphoserine useful for the solid-phase peptide synthesis

2-Methylphenyl and 2,6-dimethylphenyl groups on phosphate moiety of O-phosphoserine were more stable in HF treatment than phenyl group and could be effectively removed by hydrogenolysis. They were shown to be protective groups for phosphoserine practicall