Description

N,N-Dimethyl-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine hydrochloride (CAS: 1036991-19-1) is a highly specialized boronic ester derivative designed for advanced synthetic and medicinal chemistry applications. With the molecular formula C₁₅H₂₅BClNO₂, this compound features a pinacol-protected boronic acid group coupled with a tertiary amine moiety, making it a versatile intermediate for Suzuki-Miyaura cross-coupling reactions and other organoboron transformations. The hydrochloride salt enhances stability and solubility, ensuring reliable performance in aqueous and organic solvents. This high-purity reagent is ideal for pharmaceutical research, materials science, and catalysis, offering exceptional reactivity for C-C bond formation. Supplied as a white to off-white crystalline powder with >95% purity (HPLC), it is rigorously tested for consistency and stored under optimal conditions to maintain integrity.

Properties

• CAS Number: 1036991-19-1
• Complexity: 301
• IUPAC Name: N,N-dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine;hydrochloride
• InChI: InChI=1S/C15H24BNO2.ClH/c1-14(2)15(3,4)19-16(18-14)13-9-7-8-12(10-13)11-17(5)6;/h7-10H,11H2,1-6H3;1H
• InChI Key: DGNKUKSUIDITDJ-UHFFFAOYSA-N
• Exact Mass: 297.1666869
• Molecular Formula: C15H25BClNO2
• Molecular Weight: 297.6
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC=C2)CN(C)C.Cl
• Topological: 21.7
• Monoisotopic Mass: 297.1666869
• Synonyms: 1036991-19-1, N,N-Dimethyl-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine hydrochloride, 3-(N,N-DIMETHYLAMINO)METHYLPHENYLBORONIC ACID, PINACOL ESTER, HCL, N,N-dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine;hydrochloride, N,N-Dimethyl-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxa-borolan-2-yl)phenyl)methanamine hydrochloride, 3-[(DIMETHYLAMINO)METHYL]BENZENEBORONIC ACID, PINACOL ESTER HYDROCHLORIDE, DIMETHYL({[3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]METHYL})AMINE HYDROCHLORIDE, 3-(N,N-Dimethylaminomethy)phenylboronic acid pinacol ester hydrochloride, N,N-Dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine hydrochloride, MFCD06657878, 3-((N,N-DIMETHYLAMINO)METHYL)PHENYL BORONIC ACID PINACOL ESTER HYDROCHLORIDE, SCHEMBL2006790, DTXSID30657006, DGNKUKSUIDITDJ-UHFFFAOYSA-N, 3-(n,n-dimethylamino)methylphenylboronic acid pinacol ester hcl, 3-[(N,N-Dimethylamino)methyl]benzeneboronic acid pinacol ester hydrochloride, AKOS016004778, AB25707, PS-9694, 3-((N,N-DIMETHYLAMINO)METHY)PHENYL BORONIC ACID PINACOL ESTER HYDROCHLORIDE, DA-48175, N,N-Dimethyl-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanaminehydrochloride, CS-0175660, 3-(N,N-Dimethylamino)methylphenylboronic acid,pinacol ester,hcl, 3-(N,N dimethylaminomethyl)phenylboronic acid pinacol ester hydrochloride, 3-(N,N-Dimethylamino)methylphenylboronic acid, pinacol ester hydrochloride, 3-(n,n-dimethylaminomethyl)phenylboronic acid pinacol ester hydrochloride, 3-[(N,N-Dimethylamino)methyl]benzeneboronic acid, pinacol ester hydrochloride, N, N-dimethyl-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine-hydrochloride, N,N-dimethyl-1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine-hydrochloride, N,N-Dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine–hydrogen chloride (1/1)

This compound serves as a key intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and boron-containing therapeutics. Its boronic ester group enables efficient cross-coupling reactions for constructing complex aryl-aryl bonds. Applications extend to PET radiotracer development and polymer chemistry, where its amine functionality allows further derivatization. Suitable for use under inert conditions to prevent hydrolysis of the boronate ester.

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