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CAS 1256360-17-4

:

2-[4-Chloro-5-(cyclopropylmethoxy)-2-fluorophenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-[4-Chloro-5-(cyclopropylmethoxy)-2-fluorophenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its complex structure, which includes a dioxaborolane ring and various functional groups. The presence of a chloro and a fluorine atom on the aromatic ring contributes to its potential reactivity and biological activity. The cyclopropylmethoxy group adds steric hindrance and may influence the compound's solubility and interaction with biological targets. This compound is likely to exhibit properties typical of boron compounds, such as the ability to form coordination complexes and participate in various chemical reactions, including Suzuki coupling. Its unique structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the presence of multiple substituents may affect its physical properties, such as melting point, boiling point, and solubility in different solvents. Overall, this compound represents a specialized class of organic molecules with potential utility in various chemical and biological applications.
Formula:C16H21BClFO3
InChI:InChI=1S/C16H21BClFO3/c1-15(2)16(3,4)22-17(21-15)11-7-14(12(18)8-13(11)19)20-9-10-5-6-10/h7-8,10H,5-6,9H2,1-4H3
InChI key:InChIKey=JPKOOSAIHYNUSJ-UHFFFAOYSA-N
SMILES:FC=1C(=CC(OCC2CC2)=C(Cl)C1)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 2-[4-Chloro-5-(cyclopropylmethoxy)-2-fluorophenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-[4-chloro-5-(cyclopropylmethoxy)-2-fluorophenyl]-4,4,5,5-tetramethyl-
  • 4-Chloro-5-(cyclopropylmethoxy)-2-fluorophenylboronic acid, pinacol ester
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