2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

• CAT Number: L034439
• CAS Number: 83622-42-8
• Molecular Formula: C7H14BClO2
• Molecular Weight: 176.45
• Purity: ≥95%
• IUPAC Name: 2-(chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• InChI: InChI=1S/C7H14BClO2/c1-6(2)7(3,4)11-8(5-9)10-6/h5H2,1-4H3
• InChIKey: ABFNBZSUTILCRK-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)CCl

2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane（Cat No.:L034439）is a boron-containing compound with a dioxaborolane ring structure. The chloromethyl group at the 2-position makes it a versatile electrophilic reagent for use in organic synthesis. The tetramethyl groups at the 4 and 5 positions provide steric protection and enhance stability. This compound is commonly used as an intermediate in cross-coupling reactions, such as Suzuki reactions, where the boron atom can undergo nucleophilic substitution with organic nucleophiles, forming carbon-carbon bonds. It is valuable in the synthesis of pharmaceuticals, agrochemicals, and materials science applications.