102703-33-3

Basic information

• Product Name: P-HEXADECYLOXYNITROBENZENE
• Synonyms: P-NITROPHENYL HEXADECYL ETHER;P-HEXADECYLOXYNITROBENZENE;TIMTEC-BB SBB008227;1-(Hexadecyloxy)-4-nitrobenzene;4-Nitrophenyl hexadecyl ether
• CAS NO: 102703-33-3
• Molecular Formula: C₂₂H₃₇NO₃
• Molecular Weight: 363.53
• Mol File: 102703-33-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: 54-56 °C
• Boiling Point: 474.2°C at 760 mmHg
• Flash Point: 155.7°C
• Appearance: /
• Density: 0.974g/cm³
• Vapor Pressure: 1.05E-08mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: P-HEXADECYLOXYNITROBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: P-HEXADECYLOXYNITROBENZENE(102703-33-3)
• EPA Substance Registry System: P-HEXADECYLOXYNITROBENZENE(102703-33-3)

Safety Data

• Hazardous Substances Data: 102703-33-3(Hazardous Substances Data)

Usage

General Description

P-HEXADECYLOXYNITROBENZENE is a chemical compound with the molecular formula C22H35NO3. It is a nitrobenzene derivative with a hexadecyloxy group attached to the para position of the benzene ring. This chemical is commonly used as a synthetic intermediate in the production of various organic compounds, including pharmaceuticals, pesticides, and dyes. It is also used as a reagent in organic synthesis and has applications in the fields of chemistry, biochemistry, and materials science. P-HEXADECYLOXYNITROBENZENE is known for its relatively high molecular weight and its role as a building block in the production of more complex organic molecules.

InChI:InChI=1/C22H37NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20-26-22-18-16-21(17-19-22)23(24)25/h16-19H,2-15,20H2,1H3

Upstream product

• 100-02-7 4-nitro-phenol 
• 112-82-3 hexadecanyl bromide 
• 28341-54-0 4-(4-nitrophenoxy)butanoic acid 

Downstream Products

• 7502-06-9 4-hexadecyloxyaniline 
• 95808-43-8 acetic acid-(4-hexadecyloxy-anilide) 
• 1544691-36-2 C₅₂H₈₂N₄O₄ 

Relevant articles and documents

Luminescent mesogenic borondifluoride complexes with the Schiff bases containing salicylideneamines and β-enaminoketones core systems

Three new families of borondifluoride complexes 1a–c derived from salicylideneamines 2a and β-enaminoketonates 2b–c were reported, and their mesomorphic and optical properties were also investigated. One single crystal and molecular structure of nonmesogenic BF2 complex 1c (n = 10) was resolved and the geometry of the central boron atom was tetrahedron. A larger dihedral angle of 81.3° between the two phenyl rings observed in crystal lattice was attributed to the lack of liquid crystallinity. Boron complexes 1a formed monotropic SmA phases, while boron complexes 1b exhibited enantiotropic SmC mesophases. The optical property of the boron complexes was dependent on their molecular structures, and they emitted a blue–to–green emission at λmax = 476–541 nm in the solution and 488–550 nm in the solid state. This is the first group of mesogenic BF2 complexes with the Schiff bases derived from respective salicylideneamines and β-enaminoketones.

Volatility of some aromatic nitrosubstituted plasticizers for polymers

Nine derivatives of nitrophthalic acids and nitrophenols were synthesized as potential plasticizers for polymers and structurally characterized by 1H NMR and elemental analysis. The time dependences of the weight loss for the nitro derivatives

Novel organogelators based on pyrazine-2,5-dicarboxylic acid derivatives and their mesomorphic behaviors

A series of new low molecular organogelators (LMOGs) with thermotropic mesophase were synthesized via the reaction of 3,6-dimethyl-pyrazine-2,5- dicarboxylic acid with p-alkoxyl anilines. These compounds readily formed stable gels in a variety of organic solvents and their self-assembly behavior, structure-property relationship were investigated by scanning electron microscopy (SEM), X-ray diffraction (XRD), 1H nuclear magnetic resonance (1H NMR), Fourier transform infrared spectroscopy (FTIR) and ultra-violet-visible spectroscopy (UV). The results showed a combination of intra-hydrogen bonding, π-π stacking and van der Waals interaction resulted in the aggregation of the organogelators to form three-dimension fibrous networks. The gels formed were multi-responsive to environmental stimuli, such as temperature, fluorinion, and shear stress. More importantly, all the organogelators exhibited thermotropic hexagonal column mesophase as revealed by differential scanning calorimetry (DSC), polarized optical microscopy (POM), and variable temperature XRD studies. A control compound was synthesized and its gelling ability was also checked.