52577-04-5

Basic information

• Product Name: p-xylylene-α,α'-bis(phosphonic acid dimethyl ester)
• Synonyms: p-xylylene-α,α'-bis(phosphonic acid dimethyl ester)
• CAS NO: 52577-04-5
• Molecular Weight: 322.235
• Mol File: 52577-04-5.mol

Chemical Properties

• CAS DataBase Reference: p-xylylene-α,α'-bis(phosphonic acid dimethyl ester)(CAS DataBase Reference)
• NIST Chemistry Reference: p-xylylene-α,α'-bis(phosphonic acid dimethyl ester)(52577-04-5)
• EPA Substance Registry System: p-xylylene-α,α'-bis(phosphonic acid dimethyl ester)(52577-04-5)

Safety Data

• Hazardous Substances Data: 52577-04-5(Hazardous Substances Data)

Upstream product

• 623-25-6 p-Xylylene dichloride 
• 121-45-9 phosphorous acid trimethyl ester 
• 589-29-7 p-xylylene glycol 
• 623-24-5 1,4-bis(bromomethyl)benzene 

Downstream Products

• 4546-06-9 p-xylene diphosphonic acid 
• 58358-54-6 (E,E)-4-methyl-4'-(4''-methylstyryl)stilbene 
• 65614-65-5 (E,E)-1,4-bis(2'-hydroxystyryl)benzene 
• 65614-70-2 1,1'-{1,4-phenylenebis[(E)-ethen-2,1-diyl]}bis(3,4-dimethoxybenzene) 
• 65614-66-6 (E,E)-1,4-bis(3-hydroxystyryl)benzene 
• 65614-74-6 1,4-bis(2-methylprop-1-en-1-yl)benzene 
• 4546-08-1 p-xylylenediphosphonic acid tetrachloride 
• 200273-93-4 p-xylylene-α,α'-bis(phosphonic acid monomethyl ester) 
• 561062-53-1 ({4-[(1E)-2-(4-(1,3-dioxolan-2-yl)-2,5-dihexyloxyphenyl)vinyl]phenyl}methyl)dimethoxyphosphino-1-one 
• 561062-55-3 C₅₂H₇₄O₈ 
• 872466-50-7 (E,E)-1,4-bis[4-{bis(4-methoxyphenyl)amino}styryl]benzene 
• 375792-85-1 p-xylylene-α,α'-bis(phosphonic acid mono-3-[3'-nitro-4'-(tert-butyloxycarboxyamino-methyl)phenylmethyl]phenyl monomethyl ester) 
• 561062-57-5 4-((1E)-2-{4-[(1E)-2-(4-formyl-2,5-dihexyloxyphenyl)vinyl]phenyl}vinyl)-2,5-dihexyloxybenzaldehyde 
• 65614-69-9 C₂₂H₁₆Br₂O₂ 

Relevant articles and documents

Electroluminescence from a new distyrylbenzene based triazine dendrimer

We have synthesised a new distyrylbenzene cored dendrimer which utilises triazine rings to link the surface groups. It was found that methoxy surface groups were sufficient to give the dendrimer good solubility and good quality thin films could be prepared by spin-coating from solution. The dendrimer was luminescent both in solution and the solid state with the emission occurring from the core. The photoluminescence quantum yield was determined to be 31±3% in the solid state. The dendrimer was incorporated into a single layer light-emitting diode (ITO/dendrimer/Ca) and was found to emit blue light with an external quantum efficiency of 0.003%.

Phosphonic acid derivatives useful as anti-inflammatory agents

Novel acids, esters, and salts of phenyl, naphthyl, quinoxalinyl, and biphenyl bisphosphonic acids and 1,2-oxaphosphepins are described. These compounds are useful as antiinflammatory and anti-arthritic agents. Also described are known compounds of the phenyl, naphthyl, quinoxalinyl, and biphenyl bisphosphonate classes which are also useful as antiinflammatory and anti-arthritic agents. Representative compounds include [1,2-phenyldiyl]bis (methylene)bisphosphonic acid tetramethyl ester, [2,3-quinoxalindiyl]bis(methylene)bisphosphonic acid tetramethyl ester, [[3-(propyl)-4-(methoxy)-1,8-naphthalenediyl]bis(methylene)]bisphosphonic acid tetramethyl ester, [2,6-naphthalenediylbis(methylene) bisphosphonic acid tetraethyl ester, and [2,2'-biphenylenebis(methyl)]bisphosphonic acid tetramethyl ester. Representative oxaphosphepins include the preferred 3,4-dihydro-3-methoxy -7-(phenylmethoxy)-1H-naphth[1,8de][1,2]oxaphosphepin-3-oxide.

Phosphonic acid derivatives useful as anti-inflammatory agents

Novel 1,2-oxaphosphepins are useful as antiinflammatory and antiarthritic agents. A representative oxaphosphepin is 3,4-dihydro-3-methoxy-7-(phenylmethoxy)-1H-naphth[1,8de][1,2]oxaphosphepin-3-oxide.

(o-Hydroxyphenyl)methylphosphonic acids: Synthesis and Potentiometric Determinations of their pKa Values

(o-Hydroxyphenyl)methylphosphonic acids are readily obtained from o-(bromomethyl)- or o-(hydroxymethyl)phenols and trialkyl phosphites.Subsequent hydrolysis leads to the corresponding phosphonic acids.For a series of such compounds, the pKa val