146449-90-3

Basic information

• Product Name: (4-PENTYLOXYPHENYL)BORONIC ACID
• Synonyms: (4-PENTYLOXYPHENYL)BORONIC ACID;4-(N-PENTYLOXY)BENZENEBORONIC ACID;4-(N-PENTYLOXY)PHENYLBORONIC ACID;AKOS BRN-0164;4-Pentyloxyphenylboronic Acid (contains varying amounts of Anhydride)
• CAS NO: 146449-90-3
• Molecular Formula: C₁₁H₁₇BO₃
• Molecular Weight: 208.06
• Product Categories: blocks;BoronicAcids
• Mol File: 146449-90-3.mol
• Article Data: 7

Chemical Properties

• Melting Point: 98-100°C
• Boiling Point: 355.349 °C at 760 mmHg
• Flash Point: 168.71 °C
• Appearance: off-white solid
• Density: 1.066 g/cm³
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.71±0.16(Predicted)
• CAS DataBase Reference: (4-PENTYLOXYPHENYL)BORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (4-PENTYLOXYPHENYL)BORONIC ACID(146449-90-3)
• EPA Substance Registry System: (4-PENTYLOXYPHENYL)BORONIC ACID(146449-90-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 146449-90-3(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Uses

suzuki reaction

Upstream product

• 106-41-2 4-bromo-phenol 
• 30752-18-2 1-bromo-4-pentyloxybenzene 

Downstream Products

• 158938-08-0 4′′-(pentyloxy)-1,1′:4′,1′′-terphenyl-4-carboxylic acid 
• 57125-43-6 4-nitro-4'-pentoxybiphenyl 
• 1252054-98-0 1,4-bis(4-n-pentyloxyphenyl)anthraquinone 
• 1252055-04-1 1,4-bis(4-pentyloxyphenyl)-6,7-dimethylanthraquinone 

Relevant articles and documents

CYCLOHEXADIENE FULLERENE DERIVATIVES

The invention relates to novel fullerene derivatives, to methods for their preparation and educts or intermediates used therein, to mixtures and formulations containing them, to the use of the fullerene derivatives, mixtures and formulations as organic semiconductors in, or for the preparation of, organic electronic (OE) devices, especially organic photovoltaic (OPV) devices and organic photodetectors (OPD), and to OE, OPV and OPD devices comprising, or being prepared from, these fullerene derivatives, mixtures or formulations.

Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.

Toward boronate ester mesogenic structures

This article describes efforts toward the development of a new core for calamitic mesogens based upon the introduction of an extended heteroaromatic boroncontaining ring. A series of tri-catenar mesogenic boronate ester derivatives of the 2-phenyl-1,3,2-benzodioxaborole has been synthesized and characterized. The flat central core appeared to be a suitable feature for these derivatives to support anisotropic alignment. Additionally, these derivatives should possess an inherent dipole in the core. However, thermal analysis (polarized optical microscopy and differential scanning calorimetry) did not reveal any mesophases.