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  2. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    Phenyl thiocyanate and phenyl isothiocyanate are isomers. Organic thiocyanates are organic compounds containing the functional group RSCN. the organic group is attached to sulfur: R−S−C≡N has a S–C single bond and a C≡N triple bond. [1] Organic thiocyanates are valued building blocks.

  3. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    Lesser amounts of other hydrated compounds also form: e.g. Fe(SCN) 3 and [Fe(SCN) 4] −. [19] Similarly, Co 2+ gives a blue complex with thiocyanate. [20] Both the iron and cobalt complexes can be extracted into organic solvents like diethyl ether or amyl alcohol. This allows the determination of these ions even in strongly coloured solutions.

  4. Isothiocyanate - Wikipedia

    en.wikipedia.org/wiki/Isothiocyanate

    The N=C and C=S distances are 117 and 158 pm. [2] By contrast, in methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. Typical bond angles for C−N=C in aryl isothiocyanates are near 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°. [3] In both isomers the SCN angle approaches 180°.

  5. Category:Thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Category:Thiocyanates

    Organic thiocyanates; Thiocyanate; Transition metal complexes of thiocyanate; A. Ammonium thiocyanate; B. ... This page was last edited on 31 August 2022, ...

  6. Transition metal complexes of thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Thiocyanate can bind metals at either sulfur or nitrogen — it is an ambidentate ligand. Other factors, e.g. kinetics and solubility, sometimes influence the observed isomer. For example, [Co(NH 3) 5 (NCS)] 2+ is the thermodynamic isomer, but [Co(NH 3) 5 (SCN)] 2+ forms as the kinetic product of the reaction of thiocyanate salts with [Co(NH 3 ...

  7. Methyl isothiocyanate - Wikipedia

    en.wikipedia.org/wiki/Methyl_isothiocyanate

    Methyl isothiocyanate is the organosulfur compound with the formula CH 3 N=C=S. This low melting colorless solid is a powerful lachrymator. As a precursor to a variety of valuable bioactive compounds, it is the most important organic isothiocyanate in industry. [1]

  8. Trimethylsilyl isothiocyanate - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_isothiocyanate

    TMSNCS is useful reagent in organic chemistry. It is an ambident nucleophile, able to react with various alkyl halides, acetals, aldehydes, unsaturated compounds, aziridines, oxiranes, polycyclic aromatic hydrocarbons, and acetylated hexoses to form either thiocyanate or isothiocyanate structures. [6]

  9. Sodium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Sodium_thiocyanate

    Sodium thiocyanate (sometimes called sodium sulphocyanide) is the chemical compound with the formula NaSCN. This colorless deliquescent salt is one of the main sources of the thiocyanate anion . As such, it is used as a precursor for the synthesis of pharmaceuticals and other specialty chemicals . [ 2 ]