53478-04-9

Basic information

• Product Name: DIMETHYL 5-BENTYLOXY-ISOPHTHALATE
• Synonyms: DIMETHYL 5-BENTYLOXY-ISOPHTHALATE
• CAS NO: 53478-04-9
• Molecular Formula: C₁₇H₁₆O₅
• Molecular Weight: 280.3163
• Mol File: 53478-04-9.mol

Chemical Properties

• Boiling Point: 432.9°Cat760mmHg
• Flash Point: 191.3°C
• Appearance: /
• Density: 1.201g/cm³
• Vapor Pressure: 1.07E-07mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: DIMETHYL 5-BENTYLOXY-ISOPHTHALATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL 5-BENTYLOXY-ISOPHTHALATE(53478-04-9)
• EPA Substance Registry System: DIMETHYL 5-BENTYLOXY-ISOPHTHALATE(53478-04-9)

Safety Data

• Hazardous Substances Data: 53478-04-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H16O5/c1-20-16(18)13-8-14(17(19)21-2)10-15(9-13)22-11-12-6-4-3-5-7-12/h3-10H,11H2,1-2H3

Upstream product

• 109862-53-5 dimethyl 5-hydroxymethylbenzene-1,3-dicarboxylate 
• 100-39-0 benzyl bromide 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 100-44-7 benzyl chloride 
• 618-83-7 5-Hydroxyisophthalic acid 
• 100-51-6 benzyl alcohol 
• 584-08-7 potassium carbonate 

Downstream Products

• 189078-60-2 5-(benzyloxy)-isophthaloyl dichloride 
• 251912-48-8 [5-(benzyloxy)-1,3-phenylene]dimethanol 
• 1252993-30-8 bis[3-(9H-carbazol-9-yl)propyl]-5-(benzyloxy)isophthalate 
• 894094-40-7 C₃₉H₄₀O₁₁ 
• 1161867-78-2 C₅₅H₄₈O₇ 
• 1161867-80-6 C₆₃H₅₆O₁₅ 
• 894094-41-8 {3-[3-benzyloxy-5-(3,5-bis-hydroxymethyl-phenoxymethyl)-benzyloxy]-5-hydroxymethyl-phenyl}-methanol 
• 1161867-70-4 C₃₅H₃₂O₁₁ 
• 53478-05-0 3-(benzyloxy)-5-(methoxycarbonyl)benzoic acid 
• 114299-60-4 bis(pentafluorophenyl) 5-(benzyloxy)isophthalate 
• 114274-39-4 5-(benzyloxy)benzene-1,3-dicarboxylic acid 

Relevant articles and documents

PHOSPHATE DERIVATIVES AND USE THEREOF

The present invention discloses a compound with the following formula (I), or a tautomer, mesomer, racemate, enantiomer, and diastereoisomer thereof, or a mixture form thereof, or a pharmaceutically acceptable salt thereof, or a prodrug molecule thereof, wherein D is selected from: The invention further discloses the use of the compound in the preparation of drugs for preventing and/or treating cancers, and the use of the compound in the preparation of drugs for inhibiting cancer metastasis. The compound of the present invention can effectively inhibit the proliferation and metastasis of cancer cells by adjusting the acidity of a tumor microenvironment to achieve a better effect in clinical cancer treatment, and has broad application prospects.

COMPOUNDS, IN PARTICULAR FOR USE IN THE TREATMENT OF A DISEASE OR CONDITION FOR WHICH A BROMODOMAIN INHIBITOR IS INDICATED

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A systematic study of peripherally multiple aromatic ester-functionalized poly(benzyl ether) dendrons for the fabrication of organogels: Structure-property relationships and thixotropic property

A new class of peripherally multiple aromatic ester-functionalized poly(benzyl ether) dendrons and/or dendrimers with different focal point substituents, surface groups, interior structures, as well as different generations have been synthesized and their structure-property relationships with respect to their gelation ability have been investigated systematically. Most of these dendrons are able to gel organic solvents over a wide polarity range. Evident dendritic effects were observed not only in gelation capability but also in thermotropic, morphological, and rheological characterizations. It was disclosed that subtle changes in peripheral ester functionalities and interior dendritic structures affected the gelation behavior of the dendrons significantly. Among all the dendrons studied, the second- and third-generation dendrons G0G2-Me and G0G3-Me with dimethyl isophthalates (DMIP) as peripheral groups exhibited the best capability in gelation, and stable gels were formed in more than 22 aromatic and polar organic solvents. The lowest critical gelation concentration (CGC) reached 2.0 mg mL-1, indicating that approximately 1.35×104 solvent molecules could be entrapped by one dendritic molecule. Further study on driving forces in gel formation was carried out by using a combination of single-crystal/powder X-ray diffraction (XRD) analysis and concentration- dependent (CD)/temperature-dependent (TD) 1H NMR spectroscopy. The results obtained from these experiments revealed that the multiple π-π stacking of extended π-systems due to the peripheral DMIP rings, cooperatively assisted by non-conventional hydrogen-bonding, is the key contributor in the formation of the highly ordered supramolecular and fibrillar network. In addition, these dendritic organogels exhibited unexpected thixotropic-responsive properties, which make them promising candidates with potential applications in the field of intelligent soft materials. s

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Three new electron-rich metal-organic frameworks (MOF-1-MOF-3) have been synthesized by employing ligands bearing aromatic tags. The key role of the chosen aromatic tags is to enhance the π-electron density of the luminescent MOFs. Single-crystal X-ray st

Rotaxanes from tetralactams

Attempts to incorporate a tetralactam (3a) into a side-chain polyrotaxane by formation of its complex with p-tritylphenolate and reaction with poly(vinybenzyl chloride) failed, probably due to steric hindrance. However, three new small molecule model rota

Jacketed polymers with dendritic carbazole side groups and their applications in blue light-emitting diodes

Styrene-based monomers with the first- and second-generation dendronized carbazoles were synthesized by a convergent strategy. Conventional free radical polymerizations were carried out to synthesize the dendronized jacketed polymers using these two monomers. The apparent molecular weights of the two polymers determined by gel permeation chromatography were 57 000 and 34 000 g/mol, respectively. The polymers had excellent thermal stability with their 5% weight loss temperatures all above 360 °C. Their photophysical properties in solutions and films were investigated. Different solvents had negligible effects on their UV-vis or photoluminescent (PL) spectra. A 10 nm blue shift of the emission peak was observed in the PL spectra of films compared with those of solutions. After the films were annealed, the emission peaks became narrower. X-ray diffraction techniques were utilized to examine the phase structures of the dendronized jacketed polymers. The first-generation polymer formed a hexatic columnar nematic phase, while the second-generation one exhibited a columnar nematic phase. This stiff main-chain conformation and the dendritic side-group structure could reduce the intramolecular interactions and aggregations of the carbazole side groups and prevent the formation of excimers, which would be beneficial to the optoelectronic properties. The two polymers showed similar electrochemical properties. Their HOMO levels were about -5.3 eV, which was quite close to that of PEDOT:PSS. Electroluminescent (EL) devices were fabricated in two configurations. A new emission peak was found in the EL spectra compared with the PL spectra. All the devices emitted blue lights and possessed low driving voltages. An introduction of an electron-transporting layer could greatly improve the device properties. The best device could reach a luminescence of 2195 cd/m2, a current efficiency of 0.240 cd/A, and an external quantum efficiency of 0.353%.

POLYFUNCTIONAL EPOXY COMPOUND, EPOXY RESIN, CATIONIC PHOTOPOLYMERIZABLE EPOXY RESIN COMPOSITION, MICRO STRUCTURED MEMBER, PRODUCING METHOD THEREFOR AND LIQUID DISCHARGE HEAD

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Artificial transcription factors which mediate double-strand DNA Cleavage

A new family of artificial transcription factor (ATF)-based conjugates have been designed and synthesized as potent chemical nucleases. Polyamides as the important and efficient ATFs were used to modify and activate several anchor compounds. The results demonstrate that the resulting conjugates remarkably promote the rate accelerations and non-random double-strnd DNA cleavage activity. Interestingly, the cleavage activity of both the hydrolytic and oxidative agents was promoted efficiently through the modification of the ATFs.

Peripherally dimethyl isophthalate-functionalized poly(benzyl ether) dendrons: A new kind of unprecedented highly efficient organogelators

(Figure Presented) A series of poly(benzyl ether) dendrons, up to the fourth generation, decorated in their periphery with dimethyl esters were divergently synthesized and fully characterized. These dendrons were found to be unprecedented highly efficient

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