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Available Variants1 g
CHA.24012-1g
Price
€92.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.24012-1g | €92.80 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C5H3CuO2S |
|---|---|
| CAS Number | 68986-76-5 |
| Molecular Weight | 190.69 |
| NACRES | NA.22 |
| PubChem Substance ID | 24885718 |
| UNSPSC Code | 12161600 |
| MDL number | MFCD02183524 |
Safety Information Handling visibility
| pictograms |
GHS09
 GHS09
|
|---|---|
| signalword | Warning |
| hcodes | H410 |
| pcodes | P273 - P391 - P501 |
| Hazard Classifications | Aquatic Acute 1 - Aquatic Chronic 1 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
Copper(I) thiophene-2-carboxylate, with the CAS registry number 68986-76-5, is a chemical compound that has garnered significant attention in various fields of research. This compound is characterized by its unique structural properties, where a copper ion is coordinated to a thiophene-2-carboxylate ligand. The resulting complex exhibits distinct reactivity and stability, making it a valuable intermediate in organic synthesis and catalysis. Studies have explored the potential applications of copper(I) thiophene-2-carboxylate in cross-coupling reactions, where it serves as a catalyst or co-catalyst, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Furthermore, its properties make it a subject of interest in materials science and coordination chemistry, with ongoing research aimed at elucidating its behavior and potential uses in these areas. The compounds synthesis and characterization have been well-documented, providing a foundation for further investigation.
