24658-26-2

Usage

Uses

Used in Flavor Industry:
1,4-di([2H₃]methoxy)benzene is used as an ingredient for solid smoke flavouring. The deuterium labelling in 1,4-di([2H₃]methoxy)benzene allows for better tracking and analysis of its behavior in the flavoring process, which can lead to improved understanding and optimization of the flavoring compounds.
Used in Research and Development:
1,4-di([2H₃]methoxy)benzene can be employed as a research tool in various scientific fields, such as chemistry, biology, and materials science. The deuterium labelling provides a unique advantage for studying the compound's interactions with other molecules and its behavior under different conditions.
Used in Pharmaceutical Industry:
As an electron-rich arene, 1,4-di([2H₃]methoxy)benzene may have potential applications in the development of new drugs or drug candidates. The deuterium labelling can help in understanding the compound's metabolic pathways and its interactions with biological targets, which can be crucial for drug design and optimization.

Upstream product

• 15199-43-6 d6-dimethyl sulfate 
• 123-31-9 hydroquinone 
• 865-50-9 iodomethane-d3 

Downstream Products

• 951400-04-7 2,5-di([2H₃]methoxy)benzaldehyde 
• 1021684-56-9 1,4-dimethoxy-2-(2-nitropropenyl)benzene-d6 
• 54536-24-2 p-methoxyphenol-d3 
• 138002-60-5 1-(2,5-dimethoxyphenyl)-1-(2,5-phenyl)-2-methylpropane 

Relevant academic research and scientific papers

THE METHYL AND METHOXYL TORSIONAL MODES AND THE LATTICE VIBRATIONS IN THE LOW-FREQUENCY RAMAN SPECTRUM OF 1,4-DIMETHOXYBENZENE

The low-frequency (10-450 cm-1) Raman spectra of solid (at 300 K and 130 K) and liquid (at 335 K) 1,4-dimethoxybenzene-d0 and 1,4-dimethoxybenzene-d6 have been measured.The methyl and methoxyl torsional transitions have be

Synthesis of deuterium labeled (±)-2,5-dimethoxyamphetamine (DMA), (±)-4-bromo-2,5-dimethoxyamphetamine (DOB), and (±)-4- methoxyamphetamine (PMA) as internal standards for quantitative analyses by GC-MS

DMA, DOB and PMA are increasingly abused central nervous system stimulants with neurotoxic properties. In recent years, many controlled substance analogs (designer drugs) with a large variety of structures have reached the illegal market, making their ide

Synthesis of deuterium labeled phenethylamine derivatives

The synthesis of a series of five deuterium labeled phenethylamine derivatives, 4-bromo-2,5-[2H6]-dimethoxyphenethylamine (2C-B), 4-chloro-2,5-[2H6]-dimethoxyphenethylamine (2C-C), 2,5-[2H6]-dimethoxy-4-iodophenethylamine (2C-I), 2,5-[2H6]-dimethoxy-4-ethylthiophenethylamine (2C-T-2) and 2,5-[2H6]-dimethoxy-4-n-propylthiophenethylamine (2C-T-7) from 1,4-[2H6]-dimethoxybenzene is described. The isotopically labeled compounds are used as internal standards in gas chromatography-mass spectrometry (GC-MS) assays. Copyright