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2. Potassium thiocyanate - Wikipedia

   en.wikipedia.org/wiki/Potassium_thiocyanate

   Potassium thiocyanate is the chemical compound with the molecular formula KSCN. It is an important salt of the thiocyanate anion , one of the pseudohalides . The compound has a low melting point relative to most other inorganic salts.

3. Thiocyanate - Wikipedia

   en.wikipedia.org/wiki/Thiocyanate

   Thiocyanates are salts containing the thiocyanate anion [SCN] − (also known as rhodanide or rhodanate). [SCN] − is the conjugate base of thiocyanic acid . Common salts include the colourless salts potassium thiocyanate and sodium thiocyanate .

4. Organic thiocyanates - Wikipedia

   en.wikipedia.org/wiki/Organic_thiocyanates

   In methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. By contrast, N=C and C=S distances are 117 and 158 pm in isothiocyanates. [7] Typical bond angles for C−S−C are 100°. [3] By contrast C−N=C in aryl isothiocyanates is 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°.

5. 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 ]

6. Thiocyanic acid - Wikipedia

   en.wikipedia.org/wiki/Thiocyanic_acid

   The salts are composed of the thiocyanate ion ([SCN] −) and a suitable cation (e.g., potassium thiocyanate, KSCN). The esters of thiocyanic acid have the general structure R−S−C≡N, where R stands for an organyl group.

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8. Category:Thiocyanates - Wikipedia

   en.wikipedia.org/wiki/Category:Thiocyanates

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