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CAS 870718-04-0

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[3-bromo-2-(1-methylethoxy)phenyl]boronic acid

Description:
[3-bromo-2-(1-methylethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a bromine atom and an ethoxy group attached to a phenyl ring, contributing to its reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the compound's structure suggests potential applications in drug development and materials science due to its ability to interact with biological molecules. Its solubility in organic solvents and moderate stability under standard laboratory conditions make it a versatile reagent in synthetic chemistry. Safety considerations should be taken into account when handling this compound, as with all organoboron compounds, due to potential toxicity and reactivity.
Formula:C9H12BBrO3
InChI:InChI=1/C9H12BBrO3/c1-6(2)14-9-7(10(12)13)4-3-5-8(9)11/h3-6,12-13H,1-2H3
InChI key:InChIKey=FKHTXEIXJGJOCH-UHFFFAOYSA-N
SMILES:CC(C)Oc1c(cccc1Br)B(O)O
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