2-Isobutylthiophene is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of an isobutyl group at the second position of the thiophene ring contributes to its unique properties. This compound typically exhibits a colorless to pale yellow liquid form and has a distinctive aromatic odor. It is known for its role in organic synthesis and as a building block in the production of various pharmaceuticals and agrochemicals. The compound is relatively stable under standard conditions but may undergo reactions typical of thiophenes, such as electrophilic substitution. Its solubility in organic solvents makes it useful in various chemical applications. Additionally, 2-Isobutylthiophene's structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

2-Isobutylthiophene

2-Isobutylthiophene is a pyridine derivative that has been shown to have neuroprotective and antioxidant properties. 2-Isobutylthiophene was extracted from the bark of the tree with the same name. It has also been found to be a potent inhibitor of angiotensin converting enzyme (ACE) and possesses anti-inflammatory activity. In addition, 2-isobutylthiophene is thought to be a nootropic agent and may protect neurons in the brain by inhibiting the production of amyloid beta peptide. 2-Isobutylthiophene has been shown to inhibit parkinsonian symptoms induced by MPTP in mice.

CAS 32741-05-2: 2-Isobutylthiophene

2-Isobutylthiophene

Ref: 3D-FI153213