CAS 354812-16-1
:2-Thiophenecarboxamide, 3-amino-5-(4-methoxyphenyl)-
Description:
2-Thiophenecarboxamide, 3-amino-5-(4-methoxyphenyl)-, with the CAS number 354812-16-1, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxamide functional group, which contributes to its potential as a polar molecule, enhancing its solubility in various solvents. The presence of an amino group and a methoxy-substituted phenyl group indicates that it may exhibit interesting biological activity, possibly acting as a pharmaceutical agent or a ligand in coordination chemistry. The methoxy group can influence the compound's electronic properties and steric hindrance, affecting its reactivity and interaction with biological targets. Additionally, the compound's structure suggests potential for hydrogen bonding due to the amide and amino functionalities, which may play a role in its biological interactions. Overall, this compound's unique structural features make it a subject of interest in medicinal chemistry and material science.
Formula:C12H12N2O2S
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Found 4 products.
2-Thiophenecarboxamide, 3-amino-5-(4-methoxyphenyl)-
CAS:Formula:C12H12N2O2SPurity:95%Color and Shape:SolidMolecular weight:248.300880000000033-AMINO-5-(4-METHOXYPHENYL)-2-THIOPHENECARBOXAMIDE
CAS:Formula:C12H12N2O2SPurity:95%Color and Shape:Liquid, No data available.Molecular weight:248.3AA43279
CAS:AA43279 selectively activates Nav1.1, boosts fast-spiking interneuron activity, and raises sIPSCs in pyramidal neurons.Formula:C12H12N2O2SColor and Shape:SolidMolecular weight:248.3



