CAS 3782-00-1
:2,3-Dimethylbenzofuran
Description:
2,3-Dimethylbenzofuran is an organic compound characterized by its fused benzene and furan rings, with two methyl groups attached to the benzene moiety. It has a molecular formula of C10H10O, indicating it contains ten carbon atoms, ten hydrogen atoms, and one oxygen atom. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is relatively non-polar, which influences its solubility in organic solvents while being less soluble in water. 2,3-Dimethylbenzofuran is known for its potential applications in organic synthesis and as an intermediate in the production of various chemicals. Its structure allows for interesting reactivity patterns, making it a subject of study in both synthetic and medicinal chemistry. Additionally, like many aromatic compounds, it may exhibit some degree of toxicity and should be handled with care in laboratory settings. Safety data sheets should be consulted for specific handling and storage recommendations.
Formula:C10H10O
InChI:InChI=1S/C10H10O/c1-7-8(2)11-10-6-4-3-5-9(7)10/h3-6H,1-2H3
InChI key:InChIKey=YGBXXWTZWLALGR-UHFFFAOYSA-N
SMILES:CC=1C=2C(OC1C)=CC=CC2
Synonyms:- 2,3-Dimethyl-1-Benzofuran
- Benzofuran, 2,3-dimethyl-
- FEMA No. 3535
- 2,3-Dimethylbenzofuran
- 2,3-Dimethylbenzofuran
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Found 5 products.
2,3-Dimethylbenzofuran
CAS:<p>2,3-Dimethylbenzofuran is a high purity biochemical reagent that can be used in research related to life sciences.</p>Formula:C10H10OPurity:98.12%Color and Shape:SolidMolecular weight:146.192,3-Dimethylbenzofuran
CAS:<p>2,3-Dimethylbenzofuran (2,3-DBF) is a specific interaction that is an inorganic chemical. It has shown genotoxic effects, such as DNA damage and chromosomal aberrations, in hl-60 cells. 2,3-DBF can be acetylated by the activity of acetyltransferases to form 2,3-dimethylbenzoic acid (DMBA). DMBA is oxidized by cytochrome P450 enzymes to form DMBA quinone. DMBA quinone reacts with deuterium isotope to form an ionizable compound which can then be hydrolyzed into benzoic acid and methyl alcohol. The oxidation products of 2,3-DBF have been studied using analytical methods such as gas chromatography and mass spectrometry. These analyses showed the presence of acidic hydrolysis products and ionizable compounds.</p>Formula:C10H10OPurity:Min. 98 Area-%Color and Shape:Clear LiquidMolecular weight:146.19 g/mol




