Description

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine hydrochloride (CAS: 1462950-92-0) is a high-purity boronic ester derivative extensively utilized in organic synthesis and pharmaceutical research. With the molecular formula C₁₂H₂₃BClNO₂, this compound features a pinacol boronate group coupled with a tetrahydropyridine scaffold, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions. The hydrochloride salt form enhances stability and solubility, ensuring reliable performance in synthetic applications. This product is rigorously tested for quality, including HPLC, NMR, and mass spectrometry, to meet the stringent demands of researchers and industrial chemists. Ideal for constructing complex heterocycles, it is supplied in sealed packaging under inert conditions to maintain integrity.

Properties

• CAS Number: 1462950-92-0
• Complexity: 296
• IUPAC Name: 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine;hydrochloride
• InChI: InChI=1S/C12H22BNO2.ClH/c1-11(2)12(3,4)16-13(15-11)10-6-8-14(5)9-7-10;/h6H,7-9H2,1-5H3;1H
• InChI Key: UFEWYKAQBPBEFV-UHFFFAOYSA-N
• Exact Mass: 259.1510368
• Molecular Formula: C12H23BClNO2
• Molecular Weight: 259.58
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CCN(CC2)C.Cl
• Topological: 21.7
• Monoisotopic Mass: 259.1510368
• Synonyms: 1462950-92-0, 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine hydrochloride, 1-Methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester hydrochloride, SCHEMBL610389, 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine;hydrochloride, Pyridine, 1,2,3,6-tetrahydro-1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, hydrochloride (1:1), 1-Methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester, HCl, MFCD12913736, MIC95092, AKOS022175522, DS-7953, SB33709, DA-29182, EN300-258393, 1,2,3,6-Tetrahydropyridine-4-boronic acid, pinacol ester, hydrochloride., 1-Methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester HCl, 1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine hydrochloride, 1-Methyl-4-(4 pound not4 pound not5 pound not5-tetramethyl-1 pound not3 pound not2-dioxaborolan-2-yl)-1 pound not2 pound not3 pound not6-tetrahydropyridine hydrochloride, 1-METHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1,2,3,6-TETRAHYDROPYRIDINE HCL, 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridinehydrochloride

Application

This compound serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronate ester functionality enables efficient cross-coupling reactions for constructing C-C bonds in drug discovery. Researchers also employ it in the preparation of labeled compounds for biochemical studies. Suitable for both small-scale laboratory use and larger industrial applications.

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