CAS 68986-76-5 Copper(I) 2-thiophenecarboxylate

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

Defined Atom Stereocenter Count

Exact Mass

189.914973

H-Bond Acceptor

Heavy Atom Count

Monoisotopic Mass

189.914973

Rotatable Bond Count

Topological Polar Surface Area

68.4 Å²

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.