7715-19-7

Usage

Uses

Used in Pharmaceutical Industry:
2,5-Cyclohexadiene-1,4-dione, 2-(methoxymethyl)is used as a synthetic intermediate for the development of pharmaceuticals, contributing to the creation of new drugs and medicines. Its unique structure allows it to be a key component in the synthesis of complex organic molecules with potential therapeutic applications.
Used in Chemical Synthesis:
In the chemical industry, 2,5-Cyclohexadiene-1,4-dione, 2-(methoxymethyl)is used as a building block for the production of other chemicals. Its reactivity and functional groups make it suitable for various chemical reactions, leading to the formation of a wide range of compounds with different properties and uses.
Used in Agriculture:
2,5-Cyclohexadiene-1,4-dione, 2-(methoxymethyl)may be used in agricultural applications, potentially serving as a component in the development of new agrochemicals, such as pesticides or herbicides. Its properties could contribute to more effective and environmentally friendly solutions in crop protection.
Used in Materials Science:
In the field of materials science, 2,5-Cyclohexadiene-1,4-dione, 2-(methoxymethyl)could be employed in the development of new materials with specific properties. Its potential antioxidant or antimicrobial activity may be harnessed to create materials with enhanced durability, stability, or resistance to microbial growth.
Used in Antioxidant Applications:
Due to its potential antioxidant properties, 2,5-Cyclohexadiene-1,4-dione, 2-(methoxymethyl)may be used in various applications where protection against oxidative damage is required. This could include use in food preservation, cosmetic formulations, or industrial processes where oxidation can lead to degradation or spoilage.
Used in Antimicrobial Applications:
The potential antimicrobial activity of 2,5-Cyclohexadiene-1,4-dione, 2-(methoxymethyl)makes it a candidate for use in applications where control of microbial growth is necessary. This could include use in medical devices, water treatment, or as an additive in various products to prevent microbial contamination.

Upstream product

• 59907-65-2 4-methoxy-3-(methoxymethyl)phenol 
• 625-45-6 2-methoxyacetic acid 
• 106-51-4 p-benzoquinone 
• 57234-51-2 (m-hydroxybenzyl) methyl ether 
• 620-24-6 3-Hydroxybenzyl alcohol 
• 94420-56-1 methyl 2-methoxy-5-(2'-tetrahydropyranyloxy)benzoate 
• 94420-45-8 2-methoxymethyl-4-(2'-tetrahydropyranyloxy)anisol 
• 94420-57-2 2-methoxy-5-(2'-tetrahydropyranyloxy)phenylmethanol 
• 2150-46-1 Methyl 2,5-dihydroxybenzoate 
• 94420-55-0 methyl 2-hydroxy-5-(tetrahydropyranyloxy)benzoate 
• 131153-00-9 2-(methoxymethyl)-1,4-benzoquinone semiquinone radical 

Downstream Products

• 1380070-69-8 2-(methoxymethyl)cyclohexa-2,5-diene-1,4-dione oxime 
• 337906-36-2 2-(methoxymethyl)-p-phenylenediamine 

Relevant academic research and scientific papers

NEW TELESCOPING SYNTHESES OF 2-METHOXYMETHYL-P-PHENYLENEDIAMINE

The invention relates to processes for preparing 2 -methoxymethyl-p-phenylenediamine (I), cosmetically acceptable salts thereof, or mixtures thereof.

Method for dyeing keratinous fibres using an aminoindole in combination with a quinone derivative

Method for dyeing keratinous fibres, characterized in that at least one composition (A) containing at least one aminoindole in a medium appropriate for dyeing is applied to these fibres, the application of the composition (A) being preceded or followed by the application of a composition (B) containing, in a medium appropriate for dyeing, at least one quinone derivative chosen from ortho- or para-benzoquinones, ortho- or para-benzoquinone monoimines or diimines, 1,2- or 1,4-naphthoquinones, ortho- or para-benzoquinone sulphonimides, α,ω-alkylene-bis-1,4-benzoquinones, or 1,2- or 1,4-naphthoquinone monoimines or diimines, the aminoindoles and the quinone derivatives being chosen such that the difference in redox potential ΔE between the redox potential Ei of the aminoindoles, determined at pH 7 in a phosphate medium on a vitreous carbon electrode by voltametry, and the redox potential Eq of the quinone derivative, determined at pH 7 in a phosphate medium by polarography on a mercury electrode relative to the saturated calomel electrode, in such that

Process for dyeing keratinous fibres with a hydroxyindole in combination with a quinone derivative; and novel 1,4-benzoquinones

Process for dyeing keratinous fibres, comprising the step of applying to these fibres at least one composition A containing, in a medium appropriate for dyeing, at least one mono- or di-hydroxyindole the application of the composition A being preceded or followed by the application of a composition B containing, in a medium appropriate for dyeing, at least one quinone derivative chosen from ortho- or para-benzoquinones, monoimines or diimines of ortho- or para-benzoquinones, 1,2- or 1,4-naphthoquinones, sulphonimides of ortho- or para-benzoquinones, α, ω-alkylene-bis-1,4-benzoquinones, or 1,2- or 1,4-naphthoquinone-monoimines or -diimines; the mono- or di-hydroxyindoles and the quinone derivatives being chosen such that the oxidation-reduction potential difference ΔE between the oxidation-reduction potential Ei of the mono- or di-hydroxyindoles, determined at pH 7 in a phosphate medium on a vitreous carbon electrode by voltametry, and the oxidation-reduction potential Eq of the quinone derivative determined at pH 7 in a phosphate medium by polarography on a mercury electrode and relative to a saturated calomel electrode is such that

Pulse radiolytic kinetic study of the decay of α-methyl-substituted benzoquinone radical anions: A possible mechanistic model for bioreductive alkylation

Pulse radiolysis and transient absorption spectroscopy were used to kinetically characterize the decay of several α-methyl-substituted 1,4-benzoquinone radical anions. Electron attachment rates, absorption spectra, extinction coefficients, and pKa/s

Preparation of Regioselectively Protected Hydroquinones by Phosphorylation of p-Benzoquinones with Trialkyl Phosphites

The title reaction has been applied to 10 monosubstituted p-benzoquinones (Scheme 2, Table).The regioselectivity of the O-phosphorylation is influenced by bulky substituents (t-butyl and trimethylsilyl) and, electronically, by the methoxy group.The regioselectivity, which is high in nonpolar media (benzene), is lower in polar solvents (CH2Cl2 and CH3CN).The synthetic potential of this transformation, exemplified by the preparation of compounds 29 (Scheme 3) and 32 (Scheme 4), is considerably extended by applying milder methods for the phosphate hydrolysis and by using the reagent couple P(OCH3)3/trimethylsilyl chloride, which gives clean access to p-hydroxyphenyl phosphates. p-Benzoquinones 4h and 4i with strong ?-acceptor substituents react in a different way, giving phosphonates.The electronically induced regioselectivity of the O- and C-phosphorylation is in accordance with the preferences expected for the attack by a nucleophilic phosphorylation agent.