A variety of related derivatives are known, including diphenyl- and methylethylfurazan.

Great Lakes was a major producer of polybrominated diphenyl ethers.

For example treatment of benzeneselenol with bromine gives diphenyl diselenide.

Resistance to acifluorfen and other diphenyl ether herbicides has been reported.

The chemicals inside the plastic tube are a mixture of the dye and diphenyl oxalate.

Nitrofen is an herbicide of the diphenyl ether class.

The product is diphenyl diselenide as shown in this idealized equation:

One prominent application is the use of polybrominated diphenyl ethers as fire-retardants.

Since May 2009, this treaty also covers polybrominated diphenyl ethers and perfluorooctanesulfonic acid.

Diphenyl ditelluride is used as a source of PhTe in organic synthesis.

For example phenyl azide and phenylacetylene give diphenyl triazole.

The reaction is conducted around 300 C in polar aprotic solvents - such as diphenyl sulphone.

Thiophenols, especially in the presence of base is easily oxidized to diphenyl disulfide:

Stanley's work contributed to on lepracidal compounds, diphenyl stereochemistry and the chemistry of the sterols.

Frequently that group is a nitrile group but can also be boronic acid or diphenyl phosphonate.

The simplest members of this class include dimethyl carbonate and diphenyl carbonate:

The oxidation-elimination process produces a 1:1 molar ratio of benzeneseleninic acid and diphenyl diselenide.

Particular congeners, tetra- to hexabrominated diphenyl ethers, are the forms most frequently detected in wildlife and humans.

Trimethylsilyldiazomethane may be prepared from reacting (trimethylsilyl)methylmagnesium chloride with diphenyl phosphorazidate.

The main application of diphenyl ether is as a eutectic mixture with biphenyl, used as a heat transfer medium.

World production capacity of diphenyl carbonate was 254,000 tonnes in 2002, and phosgenation of phenol is the most significant route.

Polybrominated biphenyls and diphenyl Ethers/Oxides are used primarily as flame retardants.

The toxic chemicals include phthalates and polybrominated diphenyl ethers, both of which have been linked to multiple health problems including the following:

Diphenyl sulfone is an organosulfur compound with the formula (CH)SO.

Polycarbonates can be prepared by transesterifying diphenyl carbonate with bisphenol A, and phenol is a co-product.

If the six-packs are phenyls, then it's called a biphenyl.

See the Polychlorinated biphenyl page for more details of this destruction method.

This can be performed at lower temperatures with a copper catalyst, and to yield biphenyl.

The driving force for the contributing 3b is the restoration of aromaticity with the biphenyl unit.

See the page in this guide on polychlorinated biphenyl responsibilities for chemical manufacturers.

In one case it's a biphenyl, in the other case a dibenzodioxin.

But it's basically similar to a biphenyl.

Deinking practices no longer in use led to Polychlorinated biphenyl contamination of the river.

They are formed by electrophilic chlorination of biphenyl with chlorine gas.

The biphenyl motif also appears in drugs such as valsartan and telmisartan.

Hydroxylation of biphenyl oxide has been studied in C. echinulata.

Individual congeners are identified by the number and position of the chlorine atoms around the biphenyl rings.

Ongoing research is taking place into new asymmetric ligands such as one based on biphenyl and fenchol.

S. paucimobilis is able to degrade lignin-related biphenyl chemical compounds.

The cold fluid was a polychlorinated biphenyl.

The biphenyl molecule consists of two connected phenyl rings.

Pentaphenylantimony decomposes at 200 C to triphenylstibine and biphenyl.

In some cases the reaction is carried out with a catalytic amount of an electron carrier such as biphenyl or naphthalene.

Twenty-two people were exposed to polychlorinated biphenyl particles.

That biphenyl or dibenzodioxin structure-the twelve-pack-dissolves easily in fat.

However, it was later found that the correct structures were of sandwich compound type complexes and based on biphenyl not phenyl.

BaI can be reduced with lithium biphenyl, to give a highly active form of barium metal.

XPhos is an organophosphorus compound derived from biphenyl.

The Daryal contained organic pollutant polychlorinated biphenyl in its capacitors.

This enzyme participates in tyrosine metabolism and biphenyl degradation.

A variety of related derivatives are known, including diphenyl- and methylethylfurazan.

Diphenyl ether and many of its properties were first reported as early as 1901.

Great Lakes was a major producer of polybrominated diphenyl ethers.

Diphenyl ether is also used as a processing aid in the production of polyesters.

Resistance to acifluorfen and other diphenyl ether herbicides has been reported.

For example treatment of benzeneselenol with bromine gives diphenyl diselenide.

The chemicals inside the plastic tube are a mixture of the dye and diphenyl oxalate.

Nitrofen is an herbicide of the diphenyl ether class.

The product is diphenyl diselenide as shown in this idealized equation:

One prominent application is the use of polybrominated diphenyl ethers as fire-retardants.

Diphenyl ditelluride is used as a source of PhTe in organic synthesis.

Diphenyl ether is a starting material in the production of phenoxathiin via the Ferrario reaction.

Since May 2009, this treaty also covers polybrominated diphenyl ethers and perfluorooctanesulfonic acid.

Thiophenols, especially in the presence of base is easily oxidized to diphenyl disulfide:

For example phenyl azide and phenylacetylene give diphenyl triazole.

The reaction is conducted around 300 C in polar aprotic solvents - such as diphenyl sulphone.

Stanley's work contributed to on lepracidal compounds, diphenyl stereochemistry and the chemistry of the sterols.

The oxidation-elimination process produces a 1:1 molar ratio of benzeneseleninic acid and diphenyl diselenide.

Frequently that group is a nitrile group but can also be boronic acid or diphenyl phosphonate.

Diphenyl ether is the organic compound with the formula O(CH).

The simplest members of this class include dimethyl carbonate and diphenyl carbonate:

Particular congeners, tetra- to hexabrominated diphenyl ethers, are the forms most frequently detected in wildlife and humans.

Trimethylsilyldiazomethane may be prepared from reacting (trimethylsilyl)methylmagnesium chloride with diphenyl phosphorazidate.

World production capacity of diphenyl carbonate was 254,000 tonnes in 2002, and phosgenation of phenol is the most significant route.

The main application of diphenyl ether is as a eutectic mixture with biphenyl, used as a heat transfer medium.