51554-94-0

Usage

Uses

Used in Pharmaceutical Industry:
1-Bromo-4-n-nonylbenzene is used as a chemical intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1-Bromo-4-n-nonylbenzene serves as a building block for the production of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Advanced Materials:
1-Bromo-4-n-nonylbenzene is also utilized as a reactant in the production of liquid crystals and other advanced materials, which have applications in various fields, including display technologies and sensors.
It is crucial to handle 1-Bromo-4-n-nonylbenzene with care due to its potential hazards to human health and the environment. Proper safety measures and controls must be implemented to minimize risks associated with its use.

InChI:InChI=1/C15H23Br/c1-2-3-4-5-6-7-8-9-14-10-12-15(16)13-11-14/h10-13H,2-9H2,1H3

Upstream product

• 76287-61-1 1-Bromo-4-((E)-non-1-enyl)-benzene 
• 126334-26-7 1-(4-bromophenyl)nonan-1-one 
• 1081-77-2 n-nonylbenzene 
• 1122-91-4 4-bromo-benzaldehyde 
• 764-85-2 Nonanoyl chloride 
• 108-86-1 bromobenzene 
• 108-90-7 chlorobenzene 
• 693-58-3 1-Bromononane 
• 76287-56-4 1-(4-bromophenyl)-1-hydroxynonane 
• 17049-49-9 octylmagnesium bromide 

Downstream Products

• 135329-94-1 C₃₂H₄₈ 
• 1268269-70-0 N-(p-nonylphenyl)-9H-carbazole 
• 1268269-69-7 4,4'-dinonyltriphenylamine 
• 1356840-19-1 4-n-nonylbenzeneboronic acid pinacolate 
• 1173195-26-0 potassium 4-(1-nonyl)phenyltrifluoroborate 
• 76287-53-1 tris-nonylphenylphosphine oxide 
• 96355-59-8 1,2-Bis-(4-nonyl-phenyl)-ethane-1,2-dione 
• 70972-98-4 4-(n-nonyl)benzaldehyde 
• 76287-48-4 Tris-(4-nonyl-phenyl)-phosphane 

Relevant academic research and scientific papers

Synthesis and characterization of fully conjugated porphyrin tapes

meso-meso, β-β, β-β Triply-linked zinc(II) porphyrin tapes were synthesized by powerful oxidation of meso-meso-linked zinc(II) porphyrin arrays up to tetramers with DDQ-Sc(OTf)3. Coordination of butylamine to zinc(II) ions of porphyrin rings di

Bilitrienones from the chemical oxidation of dodecasubstituted porphyrins

The structure of the ring-opened product from direct oxidation of meso-tetra-arylporphyrins has been controversial for three decades. Herein we show that bilitrienones 2 are obtained from oxidation of metal-free dodecasubstituted porphyrins 1 in the prese

Novel dicarboxylic acid derivatives

The present patent application concerns new compounds of formula (I): displaying agonistic activity at sphingosine-1-phosphate (S1P) receptors, their process of preparation and their use as immunosuppressive agents.

Discotic liquid crystals of transition metal complexes, 31: Establishment of mesomorphism and thermochromism of bis[1,2-bis(4-n-alkoxyphenyl)ethane-1,2-dithiolene]nickel complexes

Two series of bis[1,2-bis(4-n-alkylphenyl)ethane-1,2-dithiolene]nickel, Cn-Ni (n= 1-12), and bis[1,2-bis(4-n-alkoxyphenyl)ethane-1,2-dithiolene]nickel, CnO-Ni(n = 1-12, 14, 16, 18), have been synthesized. Their mesomorphism, thermochromism, supramolecular structures and π-acceptor property have been investigated by using different scanning calorimetry, polarizing microscopy, temperature-dependent X-ray diffraction technique, electronic spectroscopy and cyclic voltammetry. From the X-ray diffraction and electronic spectral results, it was established that the CnO-Ni complexes for n ≤ 10 exhibit two differently colored discotic lamellar (DL) mesophases whereas none of the Cn-Ni complexes has a mesophase, and that the thermochromism (brown→green) is attributable to a slow transformation from the Ni-Ni bonded dimers to the Ni-S bonded dimers.

The Synthesis and Transition Temperatures of Some 4,4"-dialkyl- and 4,4"-Alkoxyalkyl-1,1':4',1"-terphenyls with 2,3- or 2',3'-difluoro Substituents and of their Biphenyl Analogues

The tetrakis(triphenylphosphine)palladium(o)-catalysed coupling of arylboronyc acids with aryl halides is used to prepare several 4,4"-dialkyl- and 4,4"-alkoxyalkyl-1,1':4',1"-terphenyls with 2,3- or 2',3'-difluoro substituents and their related biphenyl systems.Lithiation ortho to a 1,2-difluoroaromatic unit provides the route to the 2,3-difluoroarylboronic acids.The 2,3-difluoro substituted terphenyls are low-melting liquid crystals with wide-range Sc phases and no underlying smectic phase; these compounds are excellent hosts for ferroelectric systems.The compounds with widest Sc ranges are those with the difluoro substituents in an end ring and the compounds with difluoro substituents in the central ring show more nematic character and so are useful for ECB devices.

Preparation and Properties of Tertiary p-Alkylarylphosphines containing Straight-chain Alkyl Groups

A series of tris(p-alkylaryl)phosphines with straight-chain alkyl groups, P(p-C6H4-CnH2n+1)3 where n=2-9, have been prepared by reaction of phosphorus trichloride with the Grignard reagent derived from the corresponding p-bromoalkylbenzene.When n=2 and 3 the phosphines are crystalline solids, but for n>3 they are viscous oils up to n=9, which is a waxy solid.The phosphines have been characterised by microanalysis, and i.r., 1H and 31P n.m.r., and mass spectrometry.The p-substituted-arylphosphines are more sensitive than triphenylphosphine to air; aerial oxidation converts them exclusively into the corresponding phosphine oxides, in contrast to trialkylphosphines which are oxidised to a complex mixture of products.The complexing ability of the new phosphines (PAr3) is demonstrated by their ready displacement of 1,5-cyclo-octadiene (cod) from (M=Pd and Pt) to yield trans- and cis-, respectively.