CAS 850589-35-4

B-[4-(Aminothioxomethyl)phenyl]boronic acid

Description:

B-[4-(Aminothioxomethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an aminothioxomethyl 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 aminothioxomethyl substituent may impart additional reactivity and biological activity, potentially enhancing its utility in drug development or as a biochemical probe. The compound's solubility, stability, and reactivity can be influenced by the pH of the environment and the presence of other functional groups. As with many boronic acids, it may also participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the synthesis of complex organic molecules. Overall, B-[4-(Aminothioxomethyl)phenyl]boronic acid represents a versatile building block in chemical research and development.

Formula: C₇H₈BNO₂S

InChI: InChI=1S/C7H8BNO2S/c9-7(12)5-1-3-6(4-2-5)8(10)11/h1-4,10-11H,(H2,9,12)

InChI key: InChIKey=BZXPJWPWXCURIQ-UHFFFAOYSA-N

SMILES: B(O)(O)C1=CC=C(C(N)=S)C=C1

Synonyms:

• B-[4-(Aminothioxomethyl)phenyl]boronic acid
• Boronic acid, B-[4-(aminothioxomethyl)phenyl]-
• Boronic acid, [4-(aminothioxomethyl)phenyl]-

4-Boronophenylthiocarboxamide

CAS: 850589-35-4

Formula: C₇H₈BNO₂S

Molecular weight: 181.0199

Ref: IN-DA00IDIU