22247-66-1

Usage

Uses

Used in Polymer Synthesis:
4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is used as a building block in the synthesis of polymers for its ability to form long, flexible chains that contribute to the overall properties of the resulting polymers.
Used in Adhesives Industry:
In the adhesives industry, 4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is used as a key ingredient to enhance the adhesive properties of various formulations, leveraging its molecular structure to improve bonding strength and flexibility.
Used in Coatings Industry:
4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is utilized in the coatings industry as a component in the production of high-quality coatings. Its incorporation contributes to the durability, flexibility, and resistance of the coatings to various environmental factors.
Used in Plastics Industry:
In the plastics industry, 4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is used to improve the mechanical properties and flexibility of plastic materials, making them suitable for a broader range of applications.
Used in Liquid Crystal Materials Production:
4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is used in the production of liquid crystal materials due to its compatibility with the molecular structure of liquid crystals, which is essential for the development of advanced display technologies.
Used in Photoluminescent Polymers:
4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is also used in the creation of photoluminescent polymers, where its molecular structure plays a role in the emission of light upon exposure to certain wavelengths, finding applications in various optical and electronic devices.
Used in Drug Delivery Systems:
4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID has been studied for its potential use in drug delivery systems, where its unique properties may contribute to the controlled release and targeted delivery of therapeutic agents.
Used in Sunscreen Formulations:
Due to its UV-absorbing properties, 4,4'-[1,5-PENTANEDIYLBIS(OXY)] BISBENZOIC ACID is considered for use in sunscreen formulations to provide protection against harmful ultraviolet radiation.

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 111-24-0 1,5-dibromo-pentane 
• 99-96-7 4-hydroxy-benzoic acid 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 24124-37-6 methyl 4-{5-[4-(methoxycarbonyl)phenoxy]pentyloxy}benzoate 
• 628-76-2 1,5-dichloropentane 
• 69703-28-2 1,5-bis(4-carbethoxyphenoxy)pentane 

Downstream Products

• 102101-70-2 C₄₃H₅₂O₈ 
• 102101-71-3 C₄₁H₄₈O₈ 
• 87450-17-7 C₃₉H₄₄O₈ 
• 102101-72-4 C₃₇H₄₀O₈ 
• 102101-73-5 C₃₅H₃₆O₈ 
• 102101-74-6 C₃₃H₃₂O₈ 
• 102101-69-9 C₄₅H₅₆O₈ 

Relevant academic research and scientific papers

Fragment-based design of symmetrical bis-benzimidazoles as selective inhibitors of the trimethoprim-resistant, type II R67 dihydrofolate reductase

The continuously increasing use of trimethoprim as a common antibiotic for medical use and for prophylactic application in terrestrial and aquatic animal farming has increased its prevalence in the environment. This has been accompanied by increased drug

Bent-core dimesogenic compound and method for preparing thereof

The present invention refers to nuclear - manufacturing method relates to compounds and their [...] Image frame adjustment equipment of vehicles for farming, more specifically 5 has-substituted benzene two, the substituted with fluorine-substituted benzen

Biological evaluation of bisbenzaldehydes against four Mycobacterium species

A series of bisbenzaldehydes and structurally related analogs, conveniently synthesized via microwave-assisted reactions, were evaluated in vitro against drug susceptible and multi-drug resistant Mycobacterium tuberculosis, against virulent Mycobacterium bovis, against Mycobacterium ulcerans and against two Mycobacterium avium subspecies. Among the 33 substances that were tested, compound 12, i.e. 4,4′-[1,12-dodecanediyl(oxy)]bisbenzaldehyde, emerged as the most promising hit. Its activity was further confirmed in an intracellular growth inhibition assay of M. tb in murine J774 A.1 macrophages. None of the compounds showed significant cytotoxicity on human C3A hepatocytes in a neutral red dye uptake assay and no genotoxicity or mutagenicity was observed as demonstrated by a VITOTOX test and confirmed with a comet assay.

Zinc finger ejectors and methods of use thereof

Techniques for the chelation or ejection of Zn2+ from zinc finger peptides are disclosed, which can be useful in the treatment or control of viruses and viral diseases and malaria. The invention comprises contacting a zinc finger peptide with an effective

Antiprotozoal activities of symmetrical bishydroxamic acids

Symmetrical bishydroxamic acids along with their sodium salts containing an alkyl spacer between two aromatic rings were synthesized, and their antiparasitic activities were evaluated. Bishydroxamic acids were conveniently prepared from the alkylation of methyl 4-hydroxybenzoate with various dihalo-alkane, -alkene, and -ether followed by reaction with hydroxylamine. Surprisingly, the bishydroxamic acids and their sodium salts possess strong inhibitory activities against Plasmodium falciparum parasites with IC 50 values in the range of 0.26-3.2 μM. Bishydroxamic acid 3 and its sodium salt 12 also inhibit the growth of Leishmania donovani, albeit at higher concentrations. The corresponding biscarboxylic acids and bismethyl esters are inactive. Presumably, the ability of bishydroxamic acids to complex with metallic iron in hemoglobin may be responsible for antimalarial activity of these compounds.

FROM CONVENTIONAL TO LIQUID CRYSTALLINE POLYESTERS

To obtain liquid crystalline copolyesters with improved thermal behavior, p-acetoxybenzoyloxy-benzoic acid and a variety of dicarboxylic acids derived from p-hydroxybenzoic acid in combination with acetylated hydroquinone derivatives have been used as poly(ethylene terephthalate) (PETP) modifiers.The influence of the modifier structure on thermotropic properties of the copolyesters and results of dynamic mechanical measurements are discussed.

Synthesis and Thermotropic Properties of Twin Mesogens Containing a Polymethylene Spacer

DSC and microscopic data are presented for a thermotropic twin mesogen series.Deviations from normal trends were observed.