96693-05-9

Basic information

• Product Name: 4-N-OCTYLOXYBROMOBENZENE
• Synonyms: 4-N-OCTYLOXYBROMOBENZENE;1-BROMO-4-OCTYLOXYBENZENE;1-BROMO-4-N-OCTYLOXYBENZENE;1-(4-BROMOPHENOXY)OCTANE;P-BROMOPHENYL N-OCTYL ETHER;P-BROMOPHENYL OCTYL ETHER;P-BROMO(OCTYLOXY)BENZENE;P-OCTYLOXYBROMOBENZENE
• CAS NO: 96693-05-9
• Molecular Formula: C₁₄H₂₁BrO
• Molecular Weight: 285.22
• Mol File: 96693-05-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 135-137°C 0,5mm
• Flash Point: 135-137°C/0.5mm
• Appearance: /
• Density: 1.163 g/cm³
• Vapor Pressure: 0.000307mmHg at 25°C
• Refractive Index: 1.5180
• CAS DataBase Reference: 4-N-OCTYLOXYBROMOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-N-OCTYLOXYBROMOBENZENE(96693-05-9)
• EPA Substance Registry System: 4-N-OCTYLOXYBROMOBENZENE(96693-05-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 96693-05-9(Hazardous Substances Data)

Usage

General Description

4-N-Octyloxybromobenzene is a chemical compound with the molecular formula C14H21BrO. It is a brominated derivative of benzene with a substituent of an octyloxy group at the para position. This chemical is used as an intermediate in the synthesis of organic compounds, particularly in the production of pharmaceuticals, agrochemicals, and advanced materials. It is also used as a starting material for the synthesis of other chemicals and is often employed in research and development processes. 4-N-Octyloxybromobenzene is considered hazardous in case of ingestion, inhalation, and skin contact, and proper safety measures should be taken when handling this chemical.

InChI:InChI=1/C14H21BrO/c1-2-3-4-5-6-7-12-16-14-10-8-13(15)9-11-14/h8-11H,2-7,12H2,1H3

Upstream product

• 1818-07-1 octyloxybenzene 
• 106-41-2 4-bromo-phenol 
• 629-27-6 1-Iodooctane 
• 111-87-5 octanol 
• 111-83-1 1-bromo-octane 
• 78-93-3 butanone 

Downstream Products

• 24083-13-4 4-octyloxybenzaldehyde 
• 574729-54-7 (4'-bromo-biphenyl-4-yl)-bis-(4-octyloxy-phenyl)-amine 
• 1257226-20-2 4-(4-(octyloxy)benzyl)phenol 
• 1257226-14-4 [4-(tert-butyl-dimethylsilanoxy)phenyl]-4-(octyloxy)phenylmethanol 
• 773094-62-5 5,8-dibromo-2,3-bis[4-(octyloxy)phenyl]quinoxaline 
• 1263039-56-0 5,8-bis(hexylthiophen-2-yl)-2,3-bis(4-(octyloxy)phenyl)quinoxaline 
• 1021849-53-5 2,3-bis(4-octyloxyphenyl)-5,8-bis(5'-bromo-dithien-2-ly)quinoxaline 
• 1358763-34-4 2,3-bis(4-octyloxyphenyl)-5,8-bis(4'-hexyl-2,2'-bithiophene-5-ly)quinoxaline 
• 1358763-36-6 2,3-bis(4-octyloxyphenyl)-5,8-bis(5'-bromo-4'-hexyl-2,2'-bithiophene-5-ly)quinoxaline 
• 35763-07-6 1,2-bis[4-(octyloxy)phenyl]ethane-1,2-dione 
• 1342301-14-7 C₁₁₆H₁₆₄O₆S₃ 
• 1357168-94-5 3,4-di(4-octyloxyphenyl)-1-tosylpyrrole 
• 1357168-96-7 3,4-di(4-octyloxyphenyl)pyrrole 
• 1357168-99-0 1,3-bis(3,4-di(4-octyloxyphenyl)pyrrol-2-yl)-1,3-propanedione 

Relevant articles and documents

Synthesis and Characterization of a New Series of Paramagnetic Ferroelectric Liquid Crystalline Nitroxide Radicals

A new series of all-organic liquid-crystalline (LC) chiral radical compounds,trans-1-alkoxyphenyl-4-[(4-(4-alkoxyphenyl)-2,5-dimethylpyrrolidine-1-oxy-2-yl)-benzylideneamino]benzenes (1) with various alkyl chains, containing a chiral nitroxide unit in the mesogen core were synthesized and their LC properties were fully characterized. The enantiomerically enriched compounds (2S,5S)-1 showed N, TGBA, SmA and SmC phases, while the racemates (±)-1 exhibited N, SmA and SmC phases. The phase transition behavior and the ferroelectric properties of the SmC phase of (2S,5S)-1 differed from those of previously reported analogues with an ester group as a substitute for the imino group of (2S,5S)-1. Some of the (2S,5S)-1 series showed a temperature-dependent spontaneous polarization PS (θ) inversion. We discuss the origin of this difference in terms of their molecular structures optimized by molecular orbital calculations. The phase transition behavior supports the hypothesis that the large φ, which is defined as the angle between the molecular long axis (one of the principal axes of inertia) and the direction of the dipole moment in each molecule, results in the stabilization of the SmA (SmA) phase.

Tuning 'de Vries-like' properties in binary mixtures of liquid crystals with different molecular lengths

Smectic liquid crystals with 'de Vries-like' properties are characterized by a maximum layer contraction of ≤1% upon transition from the orthogonal SmA phase to the tilted SmC phase. We show that binary mixtures of 'de Vries-like' and conventional SmC mesogens with a molecular length ratio of 1.34 undergo a SmA-SmC phase transition with a maximum layer contraction ranging from 1.0 to 1.9% depending on the mixture composition.

Metal-containing dendrimers

This invention relates to a light emitting device which comprises at least one layer that contains an organometallic dendrimer having a core comprising a metal cation. The invention also relates to organometallic dendrimers and methods for producing the s