「acetonitrile」の共起表現(1語右で並び替え)

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共起表現

「acetonitrile」の共起表現一覧(1語右で並び替え)

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Hydrogenation of	acetonitrile, acetamide, and nitroethane affords ethylam
Other solvent such as	acetonitrile and chloroform can be used as modifiers.
N) cyclodimerization of various styrenes in	acetonitrile and acrylonitrile is described."
ively inert solvents such as chlorocarbons,	acetonitrile, and ethers.
absence of water, solutions of the salt in	acetonitrile and dimethyl sulfoxide are surprisingly sta
atively long lifetime of 600 nanoseconds in	acetonitrile and 400 ns in water.
dration of the gel pieces by treatment with	acetonitrile and subsequent swelling in the digestion bu
rts in presence of palladium(II) acetate in	acetonitrile at room temperature to the internal salt 2
N-diisopropylamino)phosphite in 95% aqueous	acetonitrile at 25oC is 200 h.
compound of the S-enantiomer is soluble in	acetonitrile but that of the R-enantiomer is not.
ble and soluble in organic solvents such as	acetonitrile, but is decomposed by water.
lly similar to the isomeric methyl cyanide (	acetonitrile), but its reactivity is very different.
	Acetonitrile can also be produced by many other methods,
toluene, ethyl acetate, acetone, ethanol,	acetonitrile, chloroform, dichloromethane, etc.) can the
of the common solvents for metal complexes	acetonitrile, DMSO, and DMF because they can be coordina
ting sulfuryl chloride with sodium azide in	acetonitrile, followed by the addition of excess imidazo
The main distributors of	acetonitrile in the world are: INEOS, Purification Techn
	Acetonitrile is a by-product from the manufacture of acr
The metabolism of	acetonitrile is much slower than that of other nitriles,
However,	acetonitrile is not bound very strongly to the copper io
I) ion is coordinated to four almost linear	acetonitrile ligands in a nearly ideal tetrahedral geome
As the coordinated	acetonitrile ligands may be displaced in other solvents,
The	acetonitrile may be removed in vacuo to obtain the desir
d the most common organic solvents used are	acetonitrile, methanol or tetrahydrofuran (THF).
Upon refluxing in a solution of	acetonitrile, Mo(CO)6 converts to its tris(acetonitrile)
action into a polar aprotic solvent such as	acetonitrile, N-methylpyrrolidone, furfural, or dimethyl
adium(II) chloride into reactive, monomeric	acetonitrile or benzonitrile complexes, followed by reac
with other components, such as methanol or	acetonitrile other pHs may be attained.
In	acetonitrile solution that is 0.1 M in NBu4PF6, the Fc+/
Most common organic solvents such as	acetonitrile, THF, chloroform, dichloromethane are howev
Production trends for	acetonitrile thus generally follow those of acrylonitril
In 1992, 32.3 million pounds (14,700 t) of	acetonitrile were produced in the US.
HMPN has a pKBH+ of 29.9 in	acetonitrile which is 12 orders of magnitude higher than
can also be purified by precipitation with	acetonitrile, with which it initially forms an insoluble

共起表現

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「acetonitrile」の共起表現一覧(1語右で並び替え)