Chemical Name: | [5-methoxycarbonyl-1-(4-methylphenyl)sulfonylpyrrol-3-yl]boronic acid |
CAS Number: | 916177-00-9 |
Product Number: | AG00H1JE(AGN-PC-0CMYR1) |
Synonyms: | |
MDL No: | |
Molecular Formula: | C13H14BNO6S |
Molecular Weight: | 323.1294 |
The (5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acid is a versatile chemical compound widely utilized in chemical synthesis processes. Its unique structure and properties make it a valuable tool in organic chemistry applications. This compound serves as a key building block for the synthesis of various biologically active molecules, pharmaceuticals, and agrochemicals. By incorporating (5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acid into synthetic pathways, chemists can introduce functional groups with precision, leading to the creation of complex organic compounds. Its reactivity with various coupling partners enhances its utility in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient construction of carbon-carbon bonds. Additionally, (5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acid plays a crucial role in the development of novel materials, dyes, and catalysts. Its significance in chemical synthesis lies in its ability to enable the preparation of structurally diverse molecules with tailored properties, thus contributing to advancements in the field of organic chemistry.