3-Thien-3-ylpropanoic acid, identified by its CAS number 16378-06-6, is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a propanoic acid functional group, indicating that it possesses both a carboxylic acid (-COOH) and a side chain derived from a thiophene. The thiophene moiety contributes to the compound's aromaticity and potential for various chemical interactions, including electrophilic substitution reactions. 3-Thien-3-ylpropanoic acid is likely to exhibit moderate solubility in polar solvents due to the presence of the carboxylic acid group, while its thiophene structure may enhance lipophilicity. The compound may have applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis, owing to its unique structural features. Additionally, its properties can be influenced by factors such as pH, temperature, and the presence of other functional groups in a given reaction environment.

3-THIEN-3-YLPROPANOIC ACID

16378-06-6: 3-(3-Thienyl)propanoic acid, 3-Thiophenepropanoic Acid, 3-(Thiophen-3-Yl)Propanoic Acid, 3-Thiophen-3-Ylpropanoate,  3-thien-3-ylpropanoic acid

3-(3-Thienyl)propanoic acid

3-(3-thienyl)propanoic acid

3-Thiophenepropanoic acid

3-(3-Thienyl)propanoic acid is a protonated form of 3-thienylacetic acid that is prepared by electropolymerization. This compound is a dipole with an enthalpic interaction, which has been shown to be thermodynamically favorable. The protonation of the 3-(3-thienyl)propanoic acid molecule takes place at the perovskite surface and leads to an exothermic reaction.

The following are examples of high-quality product descriptions for eCommerce:

Rifapentine is an anti-tuberculosis drug that belongs to the class of rifamycins. It is the most active of the rifamycins for the treatment of tuberculosis. Rifapentine inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch-clamp technique on

CAS 16378-06-6: 3-THIEN-3-YLPROPANOIC ACID

3-(3-Thienyl)propanoic acid

Ref: 54-OR951642

3-(3-thienyl)propanoic acid

Ref: 10-F309452

3-Thiophenepropanoic acid

Ref: IN-DA001UE2

3-(3-Thienyl)propanoic acid

Ref: 3D-RAA37806