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CAS 1111095-99-8

:

2-(5-Bromo-4-methyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(5-Bromo-4-methyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a thienyl substituent. The presence of bromine and methyl groups on the thienyl ring contributes to its reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The dioxaborolane moiety is known for its stability and ability to form boronate esters, making it useful in various chemical transformations, including Suzuki-Miyaura coupling. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its solubility in organic solvents enhances its utility in synthetic chemistry. The specific arrangement of substituents influences its electronic properties, which can affect its reactivity and interaction with other chemical species. Overall, this compound represents a valuable intermediate in the development of pharmaceuticals and agrochemicals, showcasing the versatility of boron-containing compounds in modern organic chemistry.
Formula:C11H16BBrO2S
InChI:InChI=1S/C11H16BBrO2S/c1-7-6-8(16-9(7)13)12-14-10(2,3)11(4,5)15-12/h6H,1-5H3
InChI key:InChIKey=BHDPHFRKQRKEPW-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(C)=C(Br)S2
Synonyms:
  • 2-(5-Bromo-4-methyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(5-bromo-4-methyl-2-thienyl)-4,4,5,5-tetramethyl-
  • 2-(5-Bromo-4-methylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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