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Copper(I) 2-thiophenecarboxylate
Catalog Number
ACM68986765-2
Product Name
Copper(I) 2-thiophenecarboxylate
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/68986-76-5.gif)
CAS
68986-76-5
Synonyms
2-Thiophenecarboxylic acid copper(I) salt
IUPAC Name
copper(1+);thiophene-2-carboxylate;
Molecular Weight
190.68
Molecular Formula
C5H3CuO2S
Canonical SMILES
C1=CSC(=C1)C(=O)[O-].[Cu+]
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
SFJMFSWCBVEHBA-UHFFFAOYSA-M
Purity
98%+
Appearance
Orange to brown to dark red powder to crystal
Complexity
97.1
Covalently-Bonded Unit Count
2
Defined Atom Stereocenter Count
0
Exact Mass
189.914973
H-Bond Acceptor
3
Heavy Atom Count
9
Monoisotopic Mass
189.914973
Rotatable Bond Count
0
Topological Polar Surface Area
68.4 Ų
UNII
7519WBL07L
Application
Copper(I) 2-thiophenecarboxylate serves multiple purposes in chemical research and synthesis. It is pivotal in exploring the xenobiotic responses to herbicide safener derivatives and plays a crucial role in the synthesis of functionalized BODIPY dye analogs. Its utility extends to facilitating orthogonal cross-coupling reactions and aiding in the preparation of the parent borondipyrromethene system. As a mediator, it enhances intermolecular cross-coupling reactions, as well as asymmetric 1,4-additions and allylation reactions, harnessing copper-mediated techniques to advance chemical synthesis and functionalization processes.
March 24, 2025
Versatile Copper(I) 2-Thiophenecarboxylate for Research
I've effectively used Copper(I) 2-thiophenecarboxylate from Alfa Chemistry for synthesizing functionalized BODIPY dye analogs. Its consistent performance in cross-coupling reactions enhances my research outcomes significantly. Highly recommend for advanced chemical synthesis studies.
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