Copper(I)-thiophene-2-carboxylate

"CuTC" redirects here. For other uses, see CUTC (disambiguation).

Copper(I)-thiophene-2-carboxylate[1]
IUPAC name Copper(I) thiophene-2-carboxylate
Other names CuTC
Identifiers
CAS number	68986-76-5
PubChem	11194830
ChemSpider	9369899 Y
Jmol-3D images	Image 1 Image 2
SMILES O=C([O-])C1=CC=CS1.[Cu+] [Cu+].[O-]C(=O)c1sccc1
InChI InChI=1S/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1 Y Key: SFJMFSWCBVEHBA-UHFFFAOYSA-M Y InChI=1/C5H4O2S.Cu/c6-5(7)4-2-1-3-8-4;/h1-3H,(H,6,7);/q;+1/p-1 Key: SFJMFSWCBVEHBA-REWHXWOFAY
Properties
Molecular formula	C5H3CuO2S
Molar mass	190.69 g mol−1
Hazards
R-phrases	R36/37/38
S-phrases	S26
Main hazards	Irritant (Xi)
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Copper(I)-thiophene-2-carboxylate or CuTC is a thiophene and a reagent in organic chemistry that especially promotes the Ullmann reaction between aryl halides.^[2]

References

1. ^ Copper(I) thiophene-2-carboxylate at Sigma-Aldrich
2. ^ Jwanro Hassan, Marc Sévignon, Christel Gozzi, Emmanuelle Schulz, and Marc Lemaire (2002). "Aryl-Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction". Chem. Rev. 102 (5): 1359–1470. doi:10.1021/cr000664r. PMID 11996540. http://pubs.acs.org/spotlight/july2002/cr000664r.pdf.