enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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

    In organic chemistry, isothiocyanate is a functional group as found in compounds with the formula R−N=C=S. Isothiocyanates are the more common isomers of thiocyanates, which have the formula R−S−C≡N.

  5. Category:Thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Category:Thiocyanates

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  6. 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]

  7. 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 ]

  8. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    Combining the names of functional groups with the names of the parent alkanes generates what is termed a systematic nomenclature for naming organic compounds. In traditional nomenclature, the first carbon atom after the carbon that attaches to the functional group is called the alpha carbon; the second, beta carbon, the third, gamma carbon, etc.

  9. Linkage isomerism - Wikipedia

    en.wikipedia.org/wiki/Linkage_isomerism

    In chemistry, linkage isomerism or ambidentate isomerism is a form of isomerism in which certain coordination compounds have the same composition but differ in their metal atom's connectivity to a ligand. Typical ligands that give rise to linkage isomers are: cyanide, CN − – isocyanide, NC −; cyanate, OCN − – isocyanate, NCO −