173392-87-5

Basic information

• Product Name: 4-(N-NONYLOXY)BENZENEBORONIC ACID
• Synonyms: 4-(N-NONYLOXY)PHENYLBORONIC ACID;4-(N-NONYLOXY)BENZENEBORONIC ACID;AKOS BRN-0178;(4-(Nonyloxy)phenyl)boronic acid
• CAS NO: 173392-87-5
• Molecular Formula: C₁₅H₂₅BO₃
• Molecular Weight: 264.17
• Mol File: 173392-87-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 408.4 °C at 760 mmHg
• Flash Point: 200.8 °C
• Appearance: /
• Density: 1.01 g/cm³
• Vapor Pressure: 2.11E-07mmHg at 25°C
• Refractive Index: 1.5
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(N-NONYLOXY)BENZENEBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N-NONYLOXY)BENZENEBORONIC ACID(173392-87-5)
• EPA Substance Registry System: 4-(N-NONYLOXY)BENZENEBORONIC ACID(173392-87-5)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 173392-87-5(Hazardous Substances Data)

Usage

General Description

4-(N-nonyloxy)benzeneboronic acid is a chemical compound with the molecular formula C16H27BO3. It is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction, which is used to form carbon-carbon bonds. 4-(N-NONYLOXY)BENZENEBORONIC ACID is known for its ability to efficiently and selectively catalyze the formation of carbon-carbon bonds, making it a valuable tool in the field of organic chemistry. It is also used in the production of various pharmaceuticals and agrochemicals. Additionally, 4-(N-nonyloxy)benzeneboronic acid has the potential for applications in materials science, including the development of functionalized polymers and advanced materials.

InChI:InChI=1/C15H25BO3/c1-2-3-4-5-6-7-8-13-19-15-11-9-14(10-12-15)16(17)18/h9-12,17-18H,2-8,13H2,1H3

Upstream product

• 121-43-7 Trimethyl borate 
• 105100-90-1 1-bromo-4-(nonyloxy)benzene 
• 693-58-3 1-Bromononane 
• 106-41-2 4-bromo-phenol 

Downstream Products

• 1187186-16-8 1,4-bis(4-nonyloxyphenyl)-6,7-dimethylanthraquinone 
• 178758-51-5 3-(4-Nonyloxy-phenyl)-cyclohex-2-enone 

Relevant articles and documents

Suzuki-Miyaura reaction of chloroarenes using Pd(PPh3) 4 as catalyst

The reactivity of a number of chloroarenes was investigated and chloro-nitroarenes were found to undergo facile arylation with Pd(PPh 3)4 / [Pd(PPh3)2Cl 2/n.PPh3] as catalyst. Furthermore, 4-chlorobenzaldehyde underwent arylation under the conditions, albeit with a higher catalyst loading.

Synthesis and Properties of Liquid Crystalline 4,4 -Dialkoxy-2'-Methyl-p-Terphenyls

A new series of laterally substituted terphenyl compounds, 4,4 -dialkoxy-2'-methyl-p-terphenyls (n = 1-12), were synthesized. Their liquid crystallinities were characterized by means of polarizing optical microscopy (POM), differential scanning calorimetry (DSC), and X-ray difraction (XRD). The influence of the length of the terminal alkoxy groups on the liquid crystalline behavior was investigated. It was found that the compounds with shorter end chains (n a smectic A mesophase is exhibited for those with longer end chains (9 = n = 12).

Synthesis and physical properties of thioester liquid crystals that exhibit an anti-ferro-anti phase sequencing

The thioester unit has been commonly used to enhance the mesophase thermal stability and phase range in numerous liquid crystal materials. In this paper we report the synthesis of a homologous series of thioesters with similar structures to AS620 {(S)-(+)