121219-21-4

Basic information

• Product Name: 1-Octylxy-2,3-difluorobenzene
• Synonyms: 1-Octylxy-2,3-difluorobenzene;1,2-Difluoro-3-(octyloxy)benzene
• CAS NO: 121219-21-4
• Molecular Formula: C₁₄H₂₀F₂O
• Molecular Weight: 242.307
• Mol File: 121219-21-4.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 286.338°C at 760 mmHg
• Flash Point: 134.469°C
• Appearance: /
• Density: 1.021g/cm³
• Vapor Pressure: 0.005mmHg at 25°C
• Refractive Index: 1.463
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-Octylxy-2,3-difluorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octylxy-2,3-difluorobenzene(121219-21-4)
• EPA Substance Registry System: 1-Octylxy-2,3-difluorobenzene(121219-21-4)

Safety Data

• Hazardous Substances Data: 121219-21-4(Hazardous Substances Data)

Usage

Description

1-Octylxy-2,3-difluorobenzene is an organic chemical compound that belongs to the aromatic hydrocarbon family. It is characterized by a benzene ring with two fluorine atoms attached and an octyl group replacing a hydrogen atom. The substitution of hydrogen with the highly electronegative fluorine atoms significantly alters the compound's properties, giving it unique physical and chemical characteristics.

Uses

Used in Chemical Synthesis:
1-Octylxy-2,3-difluorobenzene is used as a chemical intermediate for the synthesis of other chemical substances in scientific research. Its unique properties, resulting from the presence of fluorine atoms and the octyl group, make it a valuable component in the creation of various compounds.
However, it is important to note that the specific applications, toxicity, and environmental impact of 1-Octylxy-2,3-difluorobenzene are not widely studied or documented. Further research is needed to fully understand its potential uses and safety profile in different industries.

InChI:InChI=1/C14H20F2O/c1-2-3-4-5-6-7-11-17-13-10-8-9-12(15)14(13)16/h8-10H,2-7,11H2,1H3

Upstream product

• 111-83-1 1-bromo-octane 
• 121219-16-7 (2,3-difluorophenyl)boronic acid 
• 367-11-3 ortho-difluorobenzene 
• 6418-38-8 2,3-difluorophenol 

Downstream Products

• 121219-22-5 4-n-octyloxy-2,3-difluorophenyl boronic acid 
• 126162-89-8 4-octyloxy-1-[2-(trans-4-pentylcyclohexyl)-oxoethyl]-2,3-difluorobenzene 
• 210407-86-6 2,3-Difluoro-4-octyloxy-benzoic acid 4-nitro-phenyl ester 
• 210407-85-5 2,3-Difluoro-4-octyloxy-benzoic acid 4-formyl-phenyl ester 
• 210407-87-7 2,3-Difluoro-4-octyloxy-benzoic acid 4-amino-phenyl ester 
• 122265-96-7 2,3-difluoro-4-octyloxybenzoic acid 

Relevant articles and documents

Non-symmetric dimers comprising chalcone and cholesterol entities: An investigation on structure-property correlations

Four series of new dimers formed by interlinking chalcone and cholesterol mesogenic entities through spacers of varying length and parity have been synthesized and characterized by polarizing optical microscopy, differential scanning calorimetry, X-ray diffraction and electrical switching studies. The structure of the chalcone core has been systematically modified to investigate the effect of the molecular structure on the thermal behaviour of the dimers. The study demonstrates the dramatic dependence of thermal behaviour of these dimers on the nature of the chalcone as well as the length and parity of the spacer. the Partner Organisations 2014.

Influence of fluoro substituents on the mesophase behaviour of banana-shaped molecules

Three new series of bent-shaped five-ring liquid crystals, based on the ester of isophthalic acid as the central core and azomethine linkages, are presented. They differ by the number and the position of halogeno substituents on the outer rings. This lateral substitution strongly influences the type of mesophases formed. Calculations were performed to determine the modification of the distribution of charge along the different molecules.

Mesomorphic di- and tetra-fluorinated imines and their complexes with Re I

The synthesis of some di- and tetra-fluoro imine mesogens is described and their mesomorphism is compared with that of the parent, unfluorinated materials. The comparison reveals that in the fluorinated compounds, more ordered smectic phases were suppress