CAS 68986-76-5

(2-Thiophenecarboxylato-κO2,κS1)copper

Description:

(2-Thiophenecarboxylato-κO2,κS1)copper, with the CAS number 68986-76-5, is a coordination compound featuring copper as the central metal ion coordinated to a thiophenecarboxylate ligand. This compound typically exhibits characteristics associated with transition metal complexes, including distinct electronic and magnetic properties due to the presence of copper, which can exist in multiple oxidation states. The thiophenecarboxylate ligand contributes to the compound's stability and solubility, often influencing its reactivity and interaction with other molecules. The coordination of the ligand through both the oxygen and sulfur atoms allows for unique geometric arrangements, which can affect the compound's physical properties, such as color and crystallinity. Additionally, such complexes may exhibit interesting catalytic properties or biological activity, making them of interest in various fields, including materials science and medicinal chemistry. Overall, the specific characteristics of this compound can vary based on its synthesis and the conditions under which it is studied.

Formula: C₅H₃CuO₂S

InChI: InChI=1S/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1

InChI key: InChIKey=SFJMFSWCBVEHBA-UHFFFAOYSA-M

SMILES: O=C1C=2[S](C=CC2)[Cu+][O-]1

Synonyms:

• (2-Thiophenecarboxylato)copper
• (2-Thiophenecarboxylato-κO²,κS¹)copper
• (2-Thiophenecarboxylato-κO²,κS¹)copper (CuTC)
• 2-Thiophenecarboxylic acid, copper complex
• 2-Thiophenecarboxylic acid, copper(1+) salt (1:1)
• Copper 2-thienylcarboxylate
• Copper 2-thiophenecarboxylate
• Copper thiophene-2-carboxylate
• Copper(1+) thiophene-2-carboxylate
• Copper, (2-thiophenecarboxylato-O²,S¹)-
• Copper, (2-thiophenecarboxylato-κO²,κS¹)-
• Cuprous 2-thiophenecarboxylate
• Copper, (2-thiophenecarboxylato-O2,S1)-
• Copper, (2-thiophenecarboxylato-κO2,κS1)-
• Copper(I) thiophene-2-carboxylate

Copper(I) 2-Thiophenecarboxylate

CAS: 68986-76-5

Formula: C₅H₃CuO₂S

Color and Shape: Orange to Brown to Dark red powder to crystal

Molecular weight: 190.68

Ref: 3B-C2312

Copper(I) thiophene-2-carboxylate

CAS: 68986-76-5

Reactant or reagent used for studies of xenobiotic response safener derivatives, synthesis of functionalized BODIPY dye analogs, orthogonal cross-coupling reactions, preparation of parent borondipyrromethene system and Copper mediated cross-coupling. This Thermo Scientific Chemicals brand product wa

Formula: C₅H₃CuO₂S

Color and Shape: Yellow to green or red to brown, Powder

Molecular weight: 190.68

Ref: 02-H64950

Copper(I) thiophene-2-carboxylate

CAS: 68986-76-5

Formula: C₅H₃CuO₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 190.6871

Ref: IN-DA0034MS

Copper(I) thiophene-2-carboxylate

CAS: 68986-76-5

Copper(I) thiophene-2-carboxylate

Formula: C₅H₃CuO₂S

Purity: 95%

Color and Shape: brown solid

Molecular weight: 190.68711g/mol

Ref: 54-OR936291

Copper (I) thiophene-2-carboxylate

CAS: 68986-76-5

Formula: C₅H₃CuO₂S

Purity: 98%

Color and Shape: Powder or Crystalline Powder

Molecular weight: 190.68

Ref: 10-F043827

Copper(I) 2-Thiophenecarboxylate

CAS: 68986-76-5

Copper(I) 2-Thiophenecarboxylate is a copper complex that has been shown to inhibit the polymerase chain reaction. It binds to the active site of DNA polymerases, blocking the ability of these enzymes to synthesize DNA. This inhibition is irreversible and can be reversed by adding excess thiophenecarboxylate ligands. Copper(I) 2-Thiophenecarboxylate also inhibits lipid kinases, which are involved in signal transduction pathways that regulate immune responses and inflammation. The compound may have potential for the treatment of autoimmune diseases such as rheumatoid arthritis. The synthesis of this compound is an example of asymmetric synthesis.

Formula: C₅H₃CuO₂S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 190.69 g/mol

Ref: 3D-FC76063