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CAS 172732-52-4

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2-Cyanophenylboronic acid 1,3-propanediol cyclic ester

Description:
2-Cyanophenylboronic acid 1,3-propanediol cyclic ester, identified by its CAS number 172732-52-4, is a chemical compound that features a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This characteristic makes it particularly useful in various applications, including organic synthesis and medicinal chemistry. The presence of the cyanophenyl group contributes to its electronic properties, potentially enhancing its reactivity and interaction with biological targets. The cyclic ester structure, derived from 1,3-propanediol, suggests that the compound may exhibit unique solubility and stability characteristics. Generally, boronic acids are utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds, making this compound valuable in the synthesis of complex organic molecules. Additionally, the compound's properties may include moderate polarity and potential for hydrogen bonding, influencing its behavior in different solvents and environments. Overall, 2-Cyanophenylboronic acid 1,3-propanediol cyclic ester is a versatile compound with significant implications in chemical research and development.
Formula:C10H10BNO2
InChI:InChI=1/C10H10BNO2/c12-8-9-4-1-2-5-10(9)11-13-6-3-7-14-11/h1-2,4-5H,3,6-7H2
SMILES:c1ccc(c(c1)C#N)B1OCCCO1
Synonyms:
  • 2-(1,3,2-Dioxaborinan-2-Yl)Benzonitrile
  • 2-(1,3,2-Dioxaborolan-2-Yl)Benzonitrile
  • 2-Cyanophenylboronic acid 1,3-propanediol ester
  • 2-Cyanophenylboronic acid-1,3-propanediol cyclic ester
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