CAS 861965-63-1
:thiophen-3-amine oxalate
Description:
Thiophen-3-amine oxalate is a chemical compound characterized by its structure, which includes a thiophene ring substituted with an amine group at the 3-position, along with an oxalate salt formation. This compound typically exhibits properties associated with both the thiophene moiety and the amine functional group, such as potential aromaticity and basicity. The presence of the oxalate suggests that it may form a salt, which can influence its solubility and stability in various solvents. Thiophenes are known for their electronic properties, making them useful in organic electronics and materials science. Additionally, the amine group can participate in hydrogen bonding and may enhance the compound's reactivity. The oxalate component may also impart specific characteristics, such as the ability to form coordination complexes or influence the compound's interaction with biological systems. Overall, thiophen-3-amine oxalate is of interest in various fields, including organic synthesis, pharmaceuticals, and materials chemistry, due to its unique structural features and potential applications.
- Thiophen-3-Amine Hemioxalate
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Found 4 products.
3-Thiophenamine, ethanedioate
CAS:Formula:C6H7NO4SPurity:95%Color and Shape:SolidMolecular weight:189.1891Thiophen-3-amine oxalate
CAS:<p>Thiophen-3-amine oxalate is an organic compound that is used as a pharmaceutical intermediate. It is a white solid that has a melting point of 121°C, and can be obtained by reacting 3-aminophenol with formaldehyde in the presence of sodium bicarbonate. It has two functional groups, one chloride and one cromakalim. The skeleton consists of a phenyl ring and an activated nucleus. The phenyl ring is substituted by two n-substituted groups, which are represented by the diazoxide group and the formaldehyde group. The chemical formula for thiophen-3-amine oxalate is C8H5N3O4Cl2.</p>Formula:C6H7NO4SPurity:Min. 95%Molecular weight:189.19 g/mol
