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Calcium thiocyanate | C2CaN2S2 | CID 159641 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Thiocyanic acid, calcium salt. ChemSpider record containing structure, synonyms, properties, vendors and database links for Calcium 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. Mercury(II) thiocyanate was formerly used in pyrotechnics.
Thiocyanate (SCN) functions in host defense as part of the secreted lactoperoxidase (LPO) microbicidal pathway. SCN is the preferred substrate for LPO-driven catalytic reduction of hydrogen peroxide (H2O2) forming hypothiocyanous acid (HOSCN).
19 Σεπ 2017 · Compound 1-Cd consists of discrete complexes and in 2-Cd the Cd cations are linked into chains by the anionic and the organic co-ligands. In 3-Cd as well as 4-Cd the Cd cations are connected into chains by the thiocyanate anions, which are further linked into layers by the 3-HMPy co-ligands.
Definition. In chemistry, thiocyanate is the small molecule SCN − (the conjugate base of thiocyanic acid HSCN). Organic compounds containing the functional group SCN are also called thiocyanates. Thiocyanate may be an important prebiotic compound as it forms robustly from cyanide and elemental sulfur:
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. They allow to access efficiently various sulfur containing functional groups and scaffolds. [2] Synthesis.
