Description
Methyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzoate (CAS: 150033-80-0) is a high-purity boronic ester derivative extensively utilized in organic synthesis and pharmaceutical research. This compound, with the molecular formula C15H21BO4, features a pinacol-protected boronic ester group, enhancing its stability and reactivity in Suzuki-Miyaura cross-coupling reactions. Its methyl benzoate moiety further expands its versatility as a building block for constructing complex aromatic frameworks. Ideal for researchers and scientists, this product is rigorously tested to meet stringent quality standards, ensuring optimal performance in catalytic transformations, medicinal chemistry, and material science applications. Available in various quantities with detailed technical specifications, it is a reliable choice for advanced synthetic workflows.
Properties
- CAS Number: 150033-80-0
- Complexity: 343
- IUPAC Name: methyl 4-[(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]benzoate
- InChI: InChI=1S/C15H21BO4/c1-14(2)15(3,4)20-16(19-14)10-11-6-8-12(9-7-11)13(17)18-5/h6-9H,10H2,1-5H3
- InChI Key: QMZVNHRBNWDLTE-UHFFFAOYSA-N
- Exact Mass: 276.1532893
- Molecular Formula: C15H21BO4
- Molecular Weight: 276.14
- SMILES: B1(OC(C(O1)(C)C)(C)C)CC2=CC=C(C=C2)C(=O)OC
- Topological: 44.8
- Monoisotopic Mass: 276.1532893
- Synonyms: 150033-80-0, Methyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzoate, 4-(Methoxycarbonyl)benzylboronic Acid Pinacol Ester, MFCD18383373, METHYL 4-[(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)METHYL]BENZOATE, Benzoic acid, 4-[(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]-, methyl ester, (4-(METHOXYCARBONYL)BENZYL)BORONIC ACID PINACOL ESTER, SCHEMBL27228691, AKOS027251093, DS-10108, SY018017, DB-228892, Methyl4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzoate
Methyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)benzoate is widely employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds. Its stability and reactivity make it suitable for constructing pharmaceutical scaffolds and functional materials. Researchers also use it to develop boron-containing probes for biochemical studies. The compound’s compatibility with diverse reaction conditions enhances its utility in high-throughput synthesis and drug discovery.
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