AB66074
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $36.00 | $25.00 | - + | |
1g | 98% | in stock | $90.00 | $63.00 | - + | |
5g | 98% | in stock | $298.00 | $209.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB66074 |
Chemical Name: | 4-(2-Thienyl)benzaldehyde |
CAS Number: | 107834-03-7 |
Molecular Formula: | C11H8OS |
Molecular Weight: | 188.2456 |
MDL Number: | MFCD02682003 |
SMILES: | O=Cc1ccc(cc1)c1cccs1 |
4-(Thiophen-2-yl)benzaldehyde is a versatile compound widely used in chemical synthesis. This organic compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure containing both a thiophene ring and a benzaldehyde moiety offers a range of reactivity and functionalization possibilities in organic synthesis.One of the primary applications of 4-(Thiophen-2-yl)benzaldehyde is in the preparation of heterocyclic compounds. By utilizing the reactive aldehyde group and the electron-rich thiophene ring, chemists can efficiently construct complex cyclic structures through various synthetic routes such as cyclization reactions, Friedel-Crafts acylation, and Heck coupling reactions. These heterocycles are prevalent in medicinal chemistry as they often exhibit potent biological activities and can be found in many pharmaceuticals.Furthermore, 4-(Thiophen-2-yl)benzaldehyde can be used as a starting material for the synthesis of dye intermediates, functional materials, and molecular probes. Its ability to undergo diverse chemical transformations, including reduction, oxidation, and substitution reactions, makes it a valuable precursor in the development of novel compounds for a wide range of applications in materials science and chemical biology.