1111-67-7 | Cuprous thiocyanate

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$18.00	$12.00
100g	98%	in stock	$23.00	$16.00
500g	98%	in stock	$85.00	$60.00

Description

• Catalog Number: AB72239
• Chemical Name: Cuprous thiocyanate
• CAS Number: 1111-67-7
• Molecular Formula: CCuNS
• Molecular Weight: 121.6284
• MDL Number: MFCD00010980
• SMILES: [S-]C#N.[Cu+]

Computed Properties

• Complexity: 31.3
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 4
• Hydrogen Bond Acceptor Count: 2

Upstream Synthesis Route

Copper(I) thiocyanate, also known as cuprous thiocyanate, is a unique chemical compound that finds significant applications in chemical synthesis processes. Due to its distinct properties and reactivity, Copper(I) thiocyanate serves as a versatile reagent in various reactions, particularly in organic synthesis. Its ability to undergo facile redox reactions makes it a valuable tool for the preparation of a wide range of organic compounds.One of the primary applications of Copper(I) thiocyanate in chemical synthesis is its role as a catalyst in the Ullmann coupling reaction. This reaction involves the formation of carbon-carbon bonds between aryl halides, which is crucial in the synthesis of biaryls, a class of compounds widely used in the pharmaceutical and materials industries. Copper(I) thiocyanate acts as a catalyst by facilitating the reductive elimination of aryl-aryl bonds, leading to the formation of the desired biaryl products.In addition to its use in Ullmann coupling reactions, Copper(I) thiocyanate is also employed in the synthesis of heterocyclic compounds. By serving as a source of copper(I) ions, this compound can participate in various cross-coupling reactions to construct complex ring structures found in many organic molecules. The versatility of Copper(I) thiocyanate in promoting diverse chemical transformations highlights its importance in modern synthetic chemistry.Overall, Copper(I) thiocyanate plays a crucial role in the advancement of chemical synthesis by enabling the efficient construction of organic molecules with intricate structures. Its unique reactivity and catalytic properties make it a valuable asset for chemists seeking to develop novel compounds and materials for various applications.

Literature

• Mechanochemical and solution synthesis, X-ray structure and IR and 31P solid state NMR spectroscopic studies of copper(I) thiocyanate adducts with bulky monodentate tertiary phosphine ligands.

  Dalton transactions (Cambridge, England : 2003) 20120707

• A new simple method with high precision for determining the toxicity of antifouling paints on brine shrimp larvae (Artemia): first results.

  Chemosphere 20070401