CAS 162607-24-1
:B-(5-Propyl-2-thienyl)boronic acid
Description:
B-(5-Propyl-2-thienyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thienyl ring, specifically a 2-thienyl group with a propyl substituent at the 5-position. 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 thienyl moiety contributes to its electronic properties and potential reactivity, while the propyl group can influence its solubility and steric effects. B-(5-Propyl-2-thienyl)boronic acid may also participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable in the formation of carbon-carbon bonds. Additionally, the compound's stability, reactivity, and solubility can be affected by factors such as pH and the presence of other functional groups. Overall, this compound is of interest in the development of new materials and pharmaceuticals due to its unique structural features and reactivity.
Formula:C7H11BO2S
InChI:InChI=1S/C7H11BO2S/c1-2-3-6-4-5-7(11-6)8(9)10/h4-5,9-10H,2-3H2,1H3
InChI key:InChIKey=MIOBBTUIJGCBCF-UHFFFAOYSA-N
SMILES:B(O)(O)C=1SC(CCC)=CC1
Synonyms:- Boronic acid, (5-propyl-2-thienyl)-
- 5-Propylthiophene-2-boronic acid
- (5-Propylthiophen-2-yl)boronic acid
- B-(5-Propyl-2-thienyl)boronic acid
- Boronic acid, B-(5-propyl-2-thienyl)-
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