344396-18-5

Usage

Uses

Used in Organic Chemistry:
(3,5-dimethoxy-4-propan-2-yl-phenyl)methanol is used as a chemical intermediate for the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the creation of new molecules with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3,5-dimethoxy-4-propan-2-yl-phenyl)methanol is used as a precursor in the development of new drugs. Its structural features make it a valuable building block for designing molecules with potential therapeutic effects.
Used in Drug Development:
(3,5-dimethoxy-4-propan-2-yl-phenyl)methanol may be employed as a starting material for the synthesis of pharmaceutical agents. Its versatility in chemical reactions can lead to the creation of drug candidates with novel mechanisms of action or improved pharmacokinetic profiles.
Used in Chemical Synthesis:
(3,5-dimethoxy-4-propan-2-yl-phenyl)methanol is used as a reagent in chemical synthesis processes. Its ability to undergo various chemical transformations makes it a useful component in the preparation of complex organic molecules.
Used in Research and Development:
In research and development settings, (3,5-dimethoxy-4-propan-2-yl-phenyl)methanol is utilized to explore its potential applications and to understand its chemical behavior. This can lead to the discovery of new uses and the optimization of its synthesis and application processes.

Upstream product

• 99-10-5 3,5-Dihydroxybenzoic acid 
• 344396-17-4 methyl 4-isopropyl-3,5-dimethoxybenzoate 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 
• 55703-81-6 4-isopropyl-3,5-dimethoxybenzoic acid 

Downstream Products

• 141509-20-8 (E)-1,3-dimethoxy-2-(1-methylethyl)-5-(2-phenylethenyl)benzene 
• 443982-73-8 3,5-dimethoxy-4-isopropylbenzyl bromide 

Relevant academic research and scientific papers

Industrial preparation method of 3,5-dimethoxy-4-alkylbenzyl alcohol

The invention discloses an industrial preparation method of 3,5-dimethoxy-4-alkylbenzyl alcohol, belonging to the technical field of organic synthesis. According to the method, isopropyl chloride or isopropyl alcohol p-toluenesulfonate is selected, and isopropyl alcohol p-toluenesulfonate is directly subjected to Friedel-Crafts alkylation under the action of triethylamine hydrochloride ionic liquid serving as both a solvent and a catalyst; after the above reaction is finished, an organic solvent, such as methyl tert-butyl ether, is used for direct extraction and liquid separation, and the ionic liquid can be used repeatedly; sodium borohydride is directly used for reducing acyl imidazole obtained by subjecting isopropyl ester obtained in the previous stepto exchanging with imidazole in an aqueous tetrahydrofuran solution mildly (under the condition of 0-30 DEG C and without adding a catalyst); and after reduction is completed, a reduction product is directly poured into strong alkali solution with a concentration of 1-6 mol/L for quenching, and an organic phase is separated, so the 3,5-dimethoxy-4-alkylbenzyl alcohol is obtained safely and environmentally. The method is convenient and safe to operate, greatly reduces the problem of environmental pollution, and is suitable for industrial production.

Styrene derivative as well as synthesis method and application thereof

The invention relates to the technical field of organic synthesis, in particular to a styrene derivative and a synthesis method and application thereof. The invention discloses a styrene derivative with a structure as shown in a formula (I). The styrene d

Anti-inflammatory compound and application thereof

The invention relates to the technical field of chemical cosmetics or medicines, and concretely relates to an anti-inflammatory compound and an application thereof. By preparing a series of compoundswith an anti-inflammatory function, the obtained anti-inflammatory compound can be used for preparing cosmetic reagents or pharmaceutical reagents, and the cosmetic reagents and the pharmaceutical reagents are not specifically limited, for example, the cosmetics can be a smoothing toner, a nutritional toner, a massage cream, a nutritional cream, a mask, an emollient, a gel, and gel or shower gel shampoo and other washing type cosmetics, and can also be a pharmaceutical preparation product similar to lotion and cream, ointment, cream, plaster or spray and the like. The anti-inflammatory compound also can be used by sensitive skins, and also can be added into infant and child cosmetics to reduce irritation.

(E) - 2-phenyl-3 - (3,5-dimethoxy-4-cumene) method for the purification of acrylic acid

The invention discloses a purifying method of (E)-2-phenyl-3-(3,5-dimethoxy-4-isopropyl benzene) crylic acid and comprises two steps: 1, carrying out selective esterification on (E)-2-phenyl-3-(3,5-dimethoxy-4-isopropyl benzene) crylic acid with purity of

Synthesis of a Benvitimod impurity: (Z)-3,5-dihydroxy-4-isopropylstilbene

(E)-3,5-dihydroxy-4-isopropylstilbene (Benvitimod), a new medicine for the treatment of psoriasis and eczema, belongs to the hydroxystilbene family. The synthesis leads to the E-isomer, (Z)-3,5-dihydroxy-4-isopropylstilbene being present as a major impuri