38439-76-8

Usage

Uses

Used in Pharmaceutical Industry:
2,5-Dimethoxy-4-methylphenethylalcohol is used as a research chemical for understanding the effects of phenethylamine derivatives on the human body. Its psychoactive properties make it a valuable compound for studying neurological and psychiatric conditions, as well as for the development of new therapeutic agents.
Used in Chemical Research:
In the field of chemical research, 2,5-Dimethoxy-4-methylphenethylalcohol serves as a starting material or intermediate for the synthesis of more complex molecules. Its unique structure allows chemists to explore new synthetic pathways and develop novel compounds with potential applications in various industries.
Used in Analytical Chemistry:
2,5-Dimethoxy-4-methylphenethylalcohol can be used as a reference compound in analytical chemistry for the development and validation of analytical methods. Its distinct chemical properties make it suitable for testing the accuracy and precision of chromatographic, spectroscopic, and other analytical techniques.
Used in Forensic Science:
In forensic science, 2,5-Dimethoxy-4-methylphenethylalcohol may be used as a reference substance for the identification and quantification of psychoactive compounds in biological samples. Its presence in samples can provide valuable information for criminal investigations and toxicological analyses.
Used in Material Science:
Although not explicitly mentioned in the provided materials, the unique structure of 2,5-Dimethoxy-4-methylphenethylalcohol may also have potential applications in material science. Its properties could be explored for the development of new materials with specific characteristics, such as improved conductivity, stability, or reactivity.

Upstream product

• 75-21-8 oxirane 
• 13321-74-9 1-bromo-2,5-dimethoxy-4-methylbenzene 

Downstream Products

• 38439-79-1 2-(β-Carbamoyloxyaethyl)-5-methyl-1,4-benzochinon 
• 38439-81-5 2-<2-(N,N-Dimethylcarbamoyloxy)-aethyl>-5-methyl-p-benzochinon 
• 38439-83-7 2-<2-(N-Methyl-N-nitrosocarbamoyloxy)-aethyl>-5-methyl-p-benzochinon 
• 38440-00-5 Carbamic acid 2-(4-methyl-2,5-bis-methylamino-3,6-dioxo-cyclohexa-1,4-dienyl)-ethyl ester 
• 38440-01-6 Carbamic acid 2-(2,5-bis-ethylamino-4-methyl-3,6-dioxo-cyclohexa-1,4-dienyl)-ethyl ester 
• 38747-98-7 Carbamic acid 2-[2,5-bis-(2-diethylamino-ethylamino)-4-methyl-3,6-dioxo-cyclohexa-1,4-dienyl]-ethyl ester 
• 38439-78-0 2,5-Dimethoxy-4-methylphenethylcarbamat 
• 38439-82-6 Methyl-carbamic acid 2-(2,5-dimethoxy-4-methyl-phenyl)-ethyl ester 
• 38439-80-4 Dimethyl-carbamic acid 2-(2,5-dimethoxy-4-methyl-phenyl)-ethyl ester 
• 51267-07-3 (2,5-dimethoxy-4-methyl-phenyl)-acetic acid 
• 1276098-91-9 C₂₆H₂₅NO₅ 
• 1276099-45-6 C₁₅H₂₀O₄ 
• 1276099-08-1 C₁₃H₁₆O₄ 

Relevant academic research and scientific papers

Racemic and enantioselective total synthesis of heliespirones A & C

An account of the total synthesis of (±)-, (+)-heliespirone A and (±)-, (-)-heliespirone C is presented. In the first-generation total synthesis, we found rac-24a could be easily transformed to rac-heliespirones A & C in a biomimic way. Taking the disappointing diastereoselectivity of prenylation from 3 to 4, the nonselective dihydroxylation from 4 to 5 and the lenthy route in strategy A into account, we designed a different synthetic plan targeting a highly enantioselective, concise and protective-group free synthesis of heliespirones A & C. The palladium-catalyzed Michael addition and Sharpless AD played the key roles in the formation of optical lactone V, which could be easily transformed to compound I through two additional steps and the succedent operations were the same as those in the first-generation total synthesis. Our synthetic efforts indicated the bio-generation of heliespirones A & C from 24a should be a real process in nature.