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  2. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    Organic thiocyanates are hydrolyzed to thiocarbamates in the Riemschneider thiocarbamate synthesis. Electrochemical reduction typically converts thiocyanates to thioates and cyanide, although sometimes it can replace the thiocyanate group as a whole with hydride. [8] Some thiocyanates isomerize to the isothiocyanates.

  3. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    Thiocyanate [6] is known to be an important part in the biosynthesis of hypothiocyanite by a lactoperoxidase. [7] [8] [9] Thus the complete absence of thiocyanate or reduced thiocyanate [10] in the human body, (e.g., cystic fibrosis) is damaging to the human host defense system.

  4. 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 ]

  5. Mercury (II) thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Mercury(II)_thiocyanate

    Mercury(II) thiocyanate (Hg(SCN) 2) is an inorganic chemical compound, the coordination complex of Hg 2+ and the thiocyanate anion. It is a white powder. It is a white powder. It will produce a large, winding "snake" when ignited, an effect known as the Pharaoh's serpent .

  6. Transition metal complexes of thiocyanate - Wikipedia

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

    Addition of a thiocyanate salt to a solution containing ferric ions gives a deep red color. The identity of the chromophore remains unknown. [15] The reverse was also used: testing for the presence of thiocyanate by the addition of ferric salts. The 1:1 complex of thiocyanate and iron is deeply red. The effect was first reported in 1826. [16]

  7. Isothiocyanate - Wikipedia

    en.wikipedia.org/wiki/Isothiocyanate

    Allyl thiocyanate isomerizes to the isothiocyanate: [4] CH 2 =CHCH 2 SCN → CH 2 =CHCH 2 NCS. Isothiocyanates can be prepared by treating organic dithiocarbamate salts with lead nitrate or tosyl chloride. [5] [6] Synthesis of phenyl isothiocyanate. Isothiocyanates may also be accessed by the fragmentation reactions of 1,4,2-oxathiazoles. [7]

  8. Barium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Barium_thiocyanate

    Barium thiocyanate is prepared by mixing barium hydroxide and ammonium thiocyanate in water. [4] 2 NH 4 SCN + Ba(OH) 2 → Ba(SCN) 2 + 2 NH 3 + 2 H 2 O. According to X-ray crystallography, the anhydrous salt is a coordination polymer. The Ba 2+ ions are each bonded to eight thiocyanate anions, with four Ba-S and four Ba-N

  9. Ammonium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_thiocyanate

    Ammonium thiocyanate is used in the manufacture of herbicides, thiourea, and transparent artificial resins; in matches; as a stabilizing agent in photography; in various rustproofing compositions; as an adjuvant in textile dyeing and printing; as a tracer in oil fields; in the separation of hafnium from zirconium (important for the production of hafnium-free zircalloy for use in nuclear fuel ...