「acetonitrile」の共起表現(2語左で並び替え)

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共起表現

「acetonitrile」の共起表現一覧(2語左で並び替え)

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rts in presence of palladium(II) acetate in	acetonitrile at room temperature to the internal salt 2
toluene, ethyl acetate, acetone, ethanol,	acetonitrile, chloroform, dichloromethane, etc.) can the
Hypofluorous acid in	acetonitrile (generated in situ by passing gaseous fluor
I) ion is coordinated to four almost linear	acetonitrile ligands in a nearly ideal tetrahedral geome
ively inert solvents such as chlorocarbons,	acetonitrile, and ethers.
ting sulfuryl chloride with sodium azide in	acetonitrile, followed by the addition of excess imidazo
ree of these CO ligands can be displaced by	acetonitrile.
The main distributors of	acetonitrile in the world are: INEOS, Purification Techn
ight: 1. water, 2. methanol, 3. ethanol, 4.	acetonitrile, 5. dimethylformamide, 6. acetone, 7. ethyl
Hydrogenation of	acetonitrile, acetamide, and nitroethane affords ethylam
The metabolism of	acetonitrile is much slower than that of other nitriles,
of the common solvents for metal complexes	acetonitrile, DMSO, and DMF because they can be coordina
with other components, such as methanol or	acetonitrile other pHs may be attained.
lly similar to the isomeric methyl cyanide (	acetonitrile), but its reactivity is very different.
atively long lifetime of 600 nanoseconds in	acetonitrile and 400 ns in water.
can also be purified by precipitation with	acetonitrile, with which it initially forms an insoluble
adium(II) chloride into reactive, monomeric	acetonitrile or benzonitrile complexes, followed by reac
absence of water, solutions of the salt in	acetonitrile and dimethyl sulfoxide are surprisingly sta
.8 kg/L, and it even has some solubility in	acetonitrile.
compound of the S-enantiomer is soluble in	acetonitrile but that of the R-enantiomer is not.
Upon refluxing in a solution of	acetonitrile, Mo(CO)6 converts to its tris(acetonitrile)
N) cyclodimerization of various styrenes in	acetonitrile and acrylonitrile is described."
Other solvent such as	acetonitrile and chloroform can be used as modifiers.
ble and soluble in organic solvents such as	acetonitrile, but is decomposed by water.
Most common organic solvents such as	acetonitrile, THF, chloroform, dichloromethane are howev
action into a polar aprotic solvent such as	acetonitrile, N-methylpyrrolidone, furfural, or dimethyl
In 1992, 32.3 million pounds (14,700 t) of	acetonitrile were produced in the US.
As the coordinated	acetonitrile ligands may be displaced in other solvents,
dration of the gel pieces by treatment with	acetonitrile and subsequent swelling in the digestion bu
Production trends for	acetonitrile thus generally follow those of acrylonitril
d the most common organic solvents used are	acetonitrile, methanol or tetrahydrofuran (THF).

共起表現

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「acetonitrile」の共起表現一覧(2語左で並び替え)