2-Methylthiophene-3-carbaldehyde is an organic compound characterized by its thiophene ring structure, which includes a methyl group and an aldehyde functional group. The presence of the thiophene ring imparts aromatic properties, contributing to its stability and reactivity. This compound typically exhibits a yellow to brown liquid appearance and has a distinctive odor, often associated with its aromatic nature. It is soluble in organic solvents, such as ethanol and ether, but has limited solubility in water due to its hydrophobic thiophene structure. The aldehyde functional group makes it reactive, particularly in condensation reactions and nucleophilic additions. 2-Methylthiophene-3-carbaldehyde is utilized in various applications, including organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. Its unique structure allows for further derivatization, making it a valuable building block in synthetic organic chemistry. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

2-methylthiophene-3-carbaldehyde

84815-20-3: 3-Thiophenecarboxaldehyde, 2-Methyl-, 2-Methylthiophene-3-Carboxaldehyde

2-Methylthiophene-3-carboxaldehyde

2-Methylthiophene-3-carboxaldehyde is an alliin ligand with a monosubstituted divinylbenzene. The nature of the substituents on the divinylbenzenes was determined by analysis. The cyclopentadienyl rings in the heterocycle were synthesized by copolymerization and characterized by chromatography. The synthetic scheme for 2-methylthiophene-3-carboxaldehyde is shown in Figure 1, and the headspace profile is shown in Figure 2.

CAS 84815-20-3: 2-methylthiophene-3-carbaldehyde

2-Methylthiophene-3-carboxaldehyde

Ref: 54-OR2624

2-Methylthiophene-3-carboxaldehyde

Ref: 3D-JDA81520

2-Methylthiophene-3-carbaldehyde

Ref: IN-DA004NF3

2-Methylthiophene-3-carbaldehyde

Ref: 10-F633354