6342-72-9

Basic information

• Product Name: DIMETHYL 2-HYDROXYTEREPHTHALATE
• Synonyms: DIMETHYL 2-HYDROXYTEREPHTHALATE;NSC46640;2-Hydroxy-terephthalic acid dimethyl ester;1,4-Benzenedicarboxylic acid, 2-hydroxy-, 1,4-dimethyl ester
• CAS NO: 6342-72-9
• Molecular Formula: C₁₀H₁₀O₅
• Molecular Weight: 210.18
• Product Categories: Esters;Phenyls & Phenyl-Het
• Mol File: 6342-72-9.mol
• Article Data: 15

Chemical Properties

• Melting Point: 92-93 °C
• Boiling Point: 327.6 °C at 760 mmHg
• Flash Point: 127.9 °C
• Appearance: /
• Density: 1.284 g/cm³
• Vapor Pressure: 0.000105mmHg at 25°C
• Refractive Index: 1.544
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 8.94±0.10(Predicted)
• CAS DataBase Reference: DIMETHYL 2-HYDROXYTEREPHTHALATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL 2-HYDROXYTEREPHTHALATE(6342-72-9)
• EPA Substance Registry System: DIMETHYL 2-HYDROXYTEREPHTHALATE(6342-72-9)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 6342-72-9(Hazardous Substances Data)

Usage

General Description

Dimethyl 2-hydroxyterephthalate, also referred to as dimethyl 2-(2-hydroxyphenyl)-1,4-benzenedicarboxylate or dimethyl 3-hydroxy-1, 4-benzenedicarboxylate, is an organic compound known to be a derivative of benzoic acid. It is categorised under the family of aromatic esters. The molecular formula of this chemical compound is C10H10O5. Its structure includes two ester functional groups (-COOCH3), attached to a central carbon atom of a benzene ring, along with a hydroxyl (-OH) functional group. It is often used as a starting material in synthesizing other chemicals in various industries, especially in polymer science and drug manufacture.

InChI:InChI=1/C10H10O5/c1-14-9(12)6-3-4-7(8(11)5-6)10(13)15-2/h3-5,11H,1-2H3

Upstream product

• 100-21-0 terephthalic acid 
• 10312-55-7 3-aminoterephthalic acid 
• 610-29-7 2-nitroterephthalic acid 
• 586-35-6 2-bromo-1,4-benzenedicarboxylic acid 
• 120-61-6 1,4-benzenedicarboxylic acid dimethyl ester 
• 5372-81-6 dimethyl aminoterephthalate 
• 67-56-1 methanol 
• 636-94-2 2-hydroxyterephthalic acid 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1309869-14-4 dimethyl 2-(6-ferrocenylhexyloxy)terephthalate 
• 181022-09-3 2-(prop-2-yn-1-yloxy)terephthalic acid 
• 181022-08-2 2-prop-2-ynyloxy-terephthalic acid dimethyl ester 
• 73289-90-4 2-hydroxy-1,4-benzenedicarboxaldehyde 
• 25906-64-3 dimethyl 2-((dimethylcarbamothioyl)oxy)terephthalate 
• 97025-41-7 2-Propoxy-terephthalsaeure-dimethylester 
• 92958-69-5 2-Ethoxy-terephthalsaeure-dimethylester 
• 74295-30-0 ethoxy-terephthalic acid 
• 92865-56-0 2-Butoxy-terephthalsaeure-dimethylester 

Relevant articles and documents

DIMER COMPOUNDS, AND USE IN BINDING TOXIC REPEATS OF RNA

Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are dimeric inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.

Alkoxy-Group-Functionalized UiO-66 as Highly Efficient Adsorbents for Hydrogen Chloride Removal from Aqueous Solution

A series of alkoxy group-functionalized UiO-66 were designed for hydrogen chloride adsorption from aqueous solution, which were characterized by various methods to verify the structures and study the adsorption mechanism. A volcano-shaped change of adsorp

DIHYDROINDENE AND TETRAHYDRONAPHTHALENE COMPOUNDS

The invention provides compounds of formula I: and salts thereof, as well as pharmaceutical compositions comprising such compounds. The compounds are useful for treating cancers, Alzheimer's disease, and conditions associated with demyelination.