
CAS 916177-00-9
:5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl-3-boronic acid
Description:
5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl-3-boronic acid is a boronic acid derivative characterized by its unique structural features, which include a pyrrole ring, a tosyl group, and a methoxycarbonyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the tosyl group enhances its reactivity and solubility in organic solvents, while the methoxycarbonyl group can serve as a protective or activating group in synthetic pathways. Additionally, the compound's boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals due to its potential for functionalization and versatility in synthetic applications.
Formula:C13H14BNO6S
Synonyms:- [5-(methoxycarbonyl)-1-(4-methylbenzenesulfonyl)-1H-pyrrol-3-yl]boronic acid
- 5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl-3-boronic acid
- (5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acid
- N-Tosyl-2-methoxycarbonylpyrrole-4-boronic acid
- 1H-Pyrrole-2-carboxylic acid, 4-borono-1-[(4-methylphenyl)sulfonyl]-, 2-methyl ester
- 4-Borono-1-[(4-methylphenyl)sulfonyl]-1H-pyrrole-2-carboxylic acid 2-methyl ester
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Found 3 products.
5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl-3-boronic acid
CAS:Formula:C13H14BNO6SPurity:97%Color and Shape:SolidMolecular weight:323.1294(5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acid
CAS:(5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acidPurity:97%Molecular weight:323.14g/mol(5-(Methoxycarbonyl)-1-tosyl-1H-pyrrol-3-yl)boronic acid
CAS:Formula:C13H14BNO6SPurity:97%Color and Shape:SolidMolecular weight:323.13


