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CAS 913835-85-5

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[4-(3-methoxypropylcarbamoyl)phenyl]boronic acid

Description:
[4-(3-Methoxypropylcarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a carbamoyl group and a methoxypropyl chain, contributing to its solubility and reactivity. The boronic acid moiety allows for potential applications in medicinal chemistry, particularly in drug development and as a building block in organic synthesis. Its structure suggests that it may participate in various chemical reactions, including Suzuki coupling, which is significant in forming carbon-carbon bonds. Additionally, the presence of the methoxy group can influence the compound's electronic properties and steric hindrance, affecting its reactivity and interaction with biological targets. Overall, [4-(3-methoxypropylcarbamoyl)phenyl]boronic acid is a versatile compound with potential applications in both synthetic and pharmaceutical chemistry.
Formula:C11H16BNO4
InChI:InChI=1/C11H16BNO4/c1-17-8-2-7-13-11(14)9-3-5-10(6-4-9)12(15)16/h3-6,15-16H,2,7-8H2,1H3,(H,13,14)
SMILES:COCCCNC(=O)c1ccc(cc1)B(O)O
Synonyms:
  • 4-(3-Methoxypropylcarbamoyl)benzeneboronic acid 98%
  • 4-(3-Methoxypropylcarbamoyl)benzeneboronic acid
  • 4-(3-METHOXYPROPYLCARBAMOYL)PHENYLBORONIC ACID
  • 4-(3-Methoxypropylcarbamoyl)benzeneboronicacid98%
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