910462-34-9

Basic information

• Product Name: 1-METHYL-4-(2-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENOXY]-ETHYL)-PIPERAZINE
• Synonyms: 1-METHYL-4-(2-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENOXY]-ETHYL)-PIPERAZINE
• CAS NO: 910462-34-9
• Molecular Formula: C₁₉H₃₁BN₂O₃
• Molecular Weight: 346.27
• Mol File: 910462-34-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 461.3±40.0 °C(Predicted)
• Appearance: /
• Density: 1.08±0.1 g/cm3(Predicted)
• PKA: 7.58±0.10(Predicted)
• CAS DataBase Reference: 1-METHYL-4-(2-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENOXY]-ETHYL)-PIPERAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHYL-4-(2-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENOXY]-ETHYL)-PIPERAZINE(910462-34-9)
• EPA Substance Registry System: 1-METHYL-4-(2-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PHENOXY]-ETHYL)-PIPERAZINE(910462-34-9)

Safety Data

• Hazardous Substances Data: 910462-34-9(Hazardous Substances Data)

Usage

Structure

Contains a piperazine ring and boron atoms
Piperazine derivative with a boron-containing group attached to a phenoxyethyl moiety

Specific Group

Tetramethyl dioxaborolan group
A boron-containing ring structure

Potential Applications

Pharmaceutical or materials science
Unique structure and properties may lead to specific uses and effects

Research Status

Further research needed
To understand its specific uses, effects, and potential applications

Upstream product

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Downstream Products

• 910461-35-7 (E)-3-(1-{4'-[2-(4-methyl-piperazin-1-yl)-ethoxy]-biphenyl-3-sulfonyl}-1H-pyrrol-3-yl)-N-(tetrahydro-pyran-2-yloxy)-acrylamide 

Relevant articles and documents

Chemoselective, Scalable Nickel-Electrocatalytic O-Arylation of Alcohols

The formation of aryl-alkyl ether bonds through cross coupling of alcohols with aryl halides represents a useful strategic departure from classical SN2 methods. Numerous tactics relying on Pd-, Cu-, and Ni-based catalytic systems have emerged over the past several years. Herein we disclose a Ni-catalyzed electrochemically driven protocol to achieve this useful transformation with a broad substrate scope in an operationally simple way. This electrochemical method does not require strong base, exogenous expensive transition metal catalysts (e.g., Ir, Ru), and can easily be scaled up in either a batch or flow setting. Interestingly, e-etherification exhibits an enhanced substrate scope over the mechanistically related photochemical variant as it tolerates tertiary amine functional groups in the alcohol nucleophile.