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1,2-Dimethoxybenzene-[3,4,5,6-d4]

General Information
Catalog: BLP-010189
CAS: 126840-15-1
Molecular Formula: C8H6D4O2
Molecular Weight: 142.19
Chemical Structure
1,2-Dimethoxybenzene-[3,4,5,6-d4]
Description 1,2-Dimethoxybenzene-[3,4,5,6-d4] is a labelled analogue of 1,2-Dimethoxybenzene. 1,2-Dimethoxybenzene is a common reagent in the synthesis.
Synonyms o-Dimethoxybenzene-3,4,5,6-d4; Veratrole-3,4,5,6-d4; Catechol Dimethyl Ether-3,4,5,6-d4; Pyrocathecol Dimethyl Ether-3,4,5,6-d4
IUPAC Name 1,2,3,4-tetradeuterio-5,6-dimethoxybenzene
Related CAS 91-16-7 (unlabelled)
Canonical SMILES COC1=CC=CC=C1OC
InChI InChI=1S/C8H10O2/c1-9-7-5-3-4-6-8(7)10-2/h3-6H,1-2H3/i3D,4D,5D,6D
InChI Key ABDKAPXRBAPSQN-LNFUJOGGSA-N
Boiling Point 206.3±8.0°C at 760 mmHg
Purity 98 atom % D
Density 1.0±0.1 g/cm3

1,2-Dimethoxybenzene-[3,4,5,6-d4] is a deuterium-labeled chemical compound that serves various applications in scientific research and industry. Here are some key applications of 1,2-Dimethoxybenzene-[3,4,5,6-d4]:

Nuclear Magnetic Resonance (NMR) Spectroscopy: 1,2-Dimethoxybenzene-[3,4,5,6-d4] is commonly used as a reference or standard compound in NMR spectroscopy. The deuterium labeling provides distinct spectral patterns that help in the precise identification and analysis of other compounds in mixtures. Researchers can trace molecular structures and interactions with high accuracy due to these stable isotopic labels.

Metabolic Studies: This compound is utilized in metabolic pathway studies involving organisms or cells. Using the deuterium-labeled version of dimethoxybenzene allows researchers to track metabolic transformations and pathways with enhanced sensitivity. This can lead to deeper insights into metabolic processes and the development of improved biochemical models.

Chemical Synthesis: In synthetic chemistry, 1,2-Dimethoxybenzene-[3,4,5,6-d4] is used as a labeled precursor or reagent. Its isotopic labeling can help study reaction mechanisms by providing a clear distinction between starting materials and products. This assists chemists in fine-tuning synthesis processes and developing novel compounds with desired properties.

Environmental Analysis: The deuterated version of dimethoxybenzene can be employed in environmental studies to trace the fate and transport of organic compounds. By analyzing isotopic signatures, scientists can better understand the degradation pathways and persistence of pollutants in various ecosystems. This technique is crucial in assessing environmental impacts and developing strategies for pollution management.

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