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CAS 371765-41-2

:

5,6,7,8-tetrahydronaphthalen-1-ylboronic acid

Description:
5,6,7,8-Tetrahydronaphthalen-1-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a tetrahydronaphthalene moiety. 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 tetrahydronaphthalene structure contributes to its hydrophobic characteristics, influencing its solubility in organic solvents. Additionally, the presence of the boronic acid group allows for participation in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. The compound is often utilized in the development of pharmaceuticals and agrochemicals due to its reactivity and ability to serve as a building block in complex organic molecules. Safety data sheets should be consulted for handling and storage guidelines, as boronic acids can pose certain hazards. Overall, 5,6,7,8-tetrahydronaphthalen-1-ylboronic acid is a versatile compound in synthetic organic chemistry.
Formula:C10H13BO2
InChI:InChI=1/C10H13BO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h3,5,7,12-13H,1-2,4,6H2
SMILES:C1CCc2c(C1)cccc2B(O)O
Synonyms:
  • Boronic acid, B-(5,6,7,8-tetrahydro-1-naphthalenyl)-
  • 5,6,7,8-Tetrahydronaphthalen-1-ylboronic acid
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