Methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate

Methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate, with the CAS number 1109284-49-2, is a highly versatile and specialized chemical compound that finds its applications in various scientific domains. This Thiophene derivative, known for its distinct properties, is a valuable asset in research and development projects, particularly in the fields of organic synthesis, material science, and pharmaceutical research.

This compound presents itself as a crystalline solid, with a molecular formula of C₁₃H₁₉BO₃S and a molecular weight of 282.16 g/mol. Its chemical structure, identified by the MDL number MFCD18427556, features a thiophene ring with a methyl group and a boronate ester substituent, as well as a methyl ester group. This unique combination of functional groups endows the compound with exceptional reactivity and selectivity, making it a valuable tool for chemists and researchers.

Applications and Potential

Methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate finds its primary applications in the following areas:

Organic Synthesis

As a versatile building block, this compound is widely employed in organic synthesis, particularly in the construction of more complex molecules. The boronate ester group allows for selective cross-coupling reactions, enabling the incorporation of the thiophene moiety into a variety of target structures. This versatility makes the compound a valuable tool for synthetic chemists exploring new molecular architectures.

Material Science

Researchers in the field of material science have recognized the potential of methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate. Its unique chemical properties can be leveraged to develop novel materials with enhanced performance characteristics, such as improved thermal stability, optical properties, or electronic behavior. These materials may find applications in areas like optoelectronics, energy storage, or advanced coatings.

Pharmaceutical Research

In the pharmaceutical industry, this compound serves as a valuable building block in the synthesis of drug candidates. The thiophene scaffold, combined with the boronate ester functionality, can be strategically incorporated into the design of new therapeutic agents. Researchers may explore the potential of this compound to target a wide range of health conditions, from neurological disorders to metabolic diseases.

Technical Specifications

• CAS Number: 1109284-49-2
• Name: Methyl 5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
• Reference Number: 54-OR361451
• Molecular Formula: C₁₃H₁₉BO₃S
• Molecular Weight: 282.16 g/mol
• MDL Number: MFCD18427556
• HS Code: 2934999090

Handling and Storage

Methyl 5-methyl-4-(4,4,5,5-tetramethyl-