2-Thiophenemethanol, 5-methyl- 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 hydroxymethyl group (-CH2OH) attached to the thiophene ring at the 2-position and a methyl group (-CH3) at the 5-position. Its molecular structure contributes to its potential applications in various fields, including pharmaceuticals and materials science. The presence of the hydroxymethyl group enhances its reactivity, making it a useful intermediate in organic synthesis. Additionally, the thiophene moiety imparts unique electronic properties, which can influence the compound's behavior in chemical reactions and interactions with biological systems. 2-Thiophenemethanol, 5-methyl- is typically a colorless to pale yellow liquid or solid, depending on the specific conditions, and it may exhibit moderate solubility in organic solvents. Safety data should be consulted for handling and storage, as with all chemical substances.

2-Thiophenemethanol, 5-methyl-

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5-Methylthiophen-2-yl)methanol is a furan that contains a sulfo group. It is an electrophilic compound with mechanisms and exchangers that are still being studied. 5-Methylthiophen-2-yl)methanol reacts with thiophene to form the sulfone, which is then converted to the methylene by alkylation. The reaction of 5-methylthiophen-2-yl)methanol with pyrrole leads to the formation of the heterocycle, which can be oxidized to form the corresponding carboxylic acid. This compound also has been shown to react with formalin and acidic conditions, as well as being able to be oxidized into formaldehyde.

CAS 63826-59-5: 2-Thiophenemethanol, 5-methyl-

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