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CAS 874460-04-5

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B-[4-[[(2-Thienylmethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-[[(2-Thienylmethyl)amino]carbonyl]phenyl]boronic acid is a boronic acid derivative characterized by its unique structural features, which include a boron atom bonded to a phenyl group and an amide linkage to a thienylmethyl group. 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 thienyl group may impart additional electronic and steric properties, influencing its reactivity and solubility. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Furthermore, this compound may exhibit biological activity, potentially serving as a scaffold for drug development. Its solubility and stability in different solvents can vary, and it may require specific conditions for optimal reactivity in synthetic applications. Overall, B-[4-[[(2-Thienylmethyl)amino]carbonyl]phenyl]boronic acid represents a versatile compound in the realm of organic and medicinal chemistry.
Formula:C12H12BNO3S
InChI:InChI=1S/C12H12BNO3S/c15-12(14-8-11-2-1-7-18-11)9-3-5-10(6-4-9)13(16)17/h1-7,16-17H,8H2,(H,14,15)
InChI key:InChIKey=NOPRZKVMGDJBDW-UHFFFAOYSA-N
SMILES:C(NCC1=CC=CS1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • B-[4-[[(2-Thienylmethyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, [4-[[(2-thienylmethyl)amino]carbonyl]phenyl]-
  • Boronic acid, B-[4-[[(2-thienylmethyl)amino]carbonyl]phenyl]-
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