909391-56-6

Basic information

• Product Name: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE
• Synonyms: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE;3-(N,N-Dimethylaminomethyl)phenylboronic acid, pinacol ester;3-Dimethylaminomethylphenylboronic acid pinacol ester;Dimethyl[[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]amine;N,N-diMethyl-1-(3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)MethanaMine;3-Dimethylaminomethylphenylboronic acid pinacol ester Dimethyl[[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]amine;N,N-dimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine;N,N-Dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methylamine
• CAS NO: 909391-56-6
• Molecular Formula: C₁₅H₂₄BNO₂
• Molecular Weight: 261.18
• Mol File: 909391-56-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 340.8±25.0 °C(Predicted)
• Appearance: /
• Density: 1.00
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.78±0.28(Predicted)
• CAS DataBase Reference: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE(909391-56-6)
• EPA Substance Registry System: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE(909391-56-6)

Safety Data

• Hazardous Substances Data: 909391-56-6(Hazardous Substances Data)

Usage

General Description

DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE is a complex organic compound that contains the elements carbon, hydrogen, nitrogen, and boron. The compound is a tertiary amine with a dimethyl substituent, as well as a dioxaborolane and a benzyl group. The presence of the dioxaborolane moiety makes this compound potentially useful in organic synthesis, as dioxaborolanes are widely used in cross-coupling reactions. The specific structure and functionality of this compound could lend itself to applications in pharmaceuticals, materials science, or other chemical industries. Further study and analysis of this chemical compound may reveal additional potential uses and properties.

Upstream product

• 124-40-3 dimethyl amine 
• 214360-74-4 2-(3-(bromomethyl)phenyl)-4,4,5,5,-tetramethyl-1,3,2-dioxaborolane 
• 103-83-3 N,N'-dimethylbenzylamine 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Relevant articles and documents

Iron-catalyzed C-H borylation of arenes

Well-defined iron bis(diphosphine) complexes are active catalysts for the dehydrogenative C-H borylation of aromatic and heteroaromatic derivatives with pinacolborane. The corresponding borylated compounds were isolated in moderate to good yields (25-73%) with a 5 mol% catalyst loading under UV irradiation (350 nm) at room temperature. Stoichiometric reactivity studies and isolation of an original trans-hydrido(boryl)iron complex, Fe(H)(Bpin)(dmpe)2, allowed us to propose a mechanism showing the role of some key catalytic species.