Chemistry:Copper(I) thiophene-2-carboxylate

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Copper(I) thiophene-2-carboxylate[1]
Copper(I)-thiophene-2-carboxylate.png
Names
IUPAC name
Copper(I) thiophene-2-carboxylate
Other names
CuTC
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 633-277-7
UNII
Properties
C5H3CuO2S
Molar mass 190.68 g·mol−1
Hazards
Main hazards Irritant
GHS pictograms GHS07: Harmful
GHS Signal word Warning
H315, H319, H335
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 1 mg/m3 (as Cu)[2]
REL (Recommended)
TWA 1 mg/m3 (as Cu)[2]
IDLH (Immediate danger)
TWA 100 mg/m3 (as Cu)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

Copper(I) thiophene-2-carboxylate or CuTC is a coordination complex derived from copper and thiophene-2-carboxylic acid. It is used as a reagent to promote the Ullmann reaction between aryl halides.[3]

CuTC catalyzed Ullmann coupling

References

  1. Copper(I) thiophene-2-carboxylate at Sigma-Aldrich
  2. 2.0 2.1 2.2 NIOSH Pocket Guide to Chemical Hazards. "#0150". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0150.html. 
  3. Shijie Zhang; Dawei Zhang; Lanny S. Liebeskind (1997). "Ambient Temperature, Ullmann-like Reductive Coupling of Aryl, Heteroaryl, and Alkenyl Halides". J. Org. Chem. 62 (8): 2312–2313. doi:10.1021/jo9700078. PMID 11671553.