52643-52-4

Basic information

• Product Name: 2,3-DIMETHOXYHYDROQUINONE
• Synonyms: DIMETHOXYHYDROQUINONE, 2,3-;2,3-DIMETHOXYHYDROQUINONE
• CAS NO: 52643-52-4
• Molecular Formula: C₈H₁₀O₄
• Molecular Weight: 170.16
• Product Categories: Anthraquinones, Hydroquinones and Quinones
• Mol File: 52643-52-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-DIMETHOXYHYDROQUINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIMETHOXYHYDROQUINONE(52643-52-4)
• EPA Substance Registry System: 2,3-DIMETHOXYHYDROQUINONE(52643-52-4)

Safety Data

• Hazardous Substances Data: 52643-52-4(Hazardous Substances Data)

Usage

General Description

2,3-DIMETHOXYHYDROQUINONE is a chemical compound that belongs to the class of organic compounds known as hydroquinones. It is a derivative of hydroquinone, a phenolic compound widely used as a reducing agent and antioxidant. 2,3-DIMETHOXYHYDROQUINONE is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used in the production of rubber and plastics. 2,3-DIMETHOXYHYDROQUINONE has antioxidant properties and has been studied for its potential therapeutic applications in the treatment of cancer, inflammation, and neurodegenerative diseases. Additionally, 2,3-DIMETHOXYHYDROQUINONE has been investigated for its potential use in the development of novel materials and electronic components due to its unique chemical and electronic properties.

Upstream product

• 5150-42-5 2,3-dimethoxyphenol 
• 3117-02-0 2,3-dimethoxy-1,4-benzoquinone 
• 5653-45-2 2,5-dihydroxy-3,4-dimethoxy-benzoic acid 
• 610-02-6 2,3,4-trihydroxybenzoic acid 
• 5653-46-3 2-hydroxy-3,4-dimethoxybenzoic acid 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 
• 30225-82-2 2,3,4-trimethoxyphenyl formate 

Downstream Products

• 3117-02-0 2,3-dimethoxy-1,4-benzoquinone 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 
• 146273-84-9 7-Hydroxy-8,9-dimethoxy-5-phenyl-4,5-dihydro-3H-benzo[b]oxepin-2-one 
• 89635-20-1 1,4-bis(benzyloxy)-2,3-dimethoxybenzene 
• 89635-21-2 3,4-dimethoxy-2,5-bis(benzyloxy)benzaldehyde 
• 89635-12-1 Acetic acid 6-[(E)-3-(2,5-bis-benzyloxy-3,4-dimethoxy-phenyl)-acryloyl]-2,3-dimethoxy-phenyl ester 
• 89635-10-9 1-(5-Benzyloxy-2-hydroxy-4-methoxyphenyl)-3-(2,5-dibenzyloxy-3,4-dimethoxyphenyl)-2-propen-1-on 
• 89635-19-8 2',5,',6-Tribenzyloxy-3',4',7,8-tetramethoxyisoflavon 
• 89635-11-0 Acetic acid 4-benzyloxy-2-[(E)-3-(2,5-bis-benzyloxy-3,4-dimethoxy-phenyl)-acryloyl]-5-methoxy-phenyl ester 

Relevant articles and documents

Bioinspired Total Synthesis of Bussealin e

The first total synthesis of bussealin E, a natural product with a unique cycloheptadibenzofuran scaffold, is reported. A strategy inspired by a proposed biosynthesis was employed whereby a diphenylpropane derivative underwent an oxidative phenolic coupling to forge the tetracyclic ring system. The synthesis of the diphenylpropane featured a key sp2-sp3 Hiyama coupling between a vinyldisiloxane and a benzylic bromide.

Synthesis of an Isotopically Labeled Naphthalene Derivative That Supports a Long-Lived Nuclear Singlet State

The synthesis of an octa-alkoxy substituted isotopically labeled naphthalene derivative, shown to have excellent properties in singlet NMR experiments, is described. This highly substituted naphthalene system, which incorporates an adjacent 13C spin pair, is readily accessed from a commercially available 13C2-labeled building block via sequential thermal alkynyl- and arylcyclobutenone rearrangements. The synthetic route incorporates a simple desymmetrization approach leading to a small difference in the chemical shifts of the 13C spin pair, a design constraint crucial for accessing nuclear singlet order. (Chemical Equation Presented).

Anti-tumuor agents

The invention concerns anti-tumour agents of formula (I) wherein each of R1, R2and R3has the meanings defined in the specification including hydrogen, (1-4C)alkyl, (3-4)alkenyl, (3-4C)alkynyl, amino, (1-4C)alkylamino and (