CAS 675-09-2

Mesitene lactone

Description:

Mesitene lactone, with the CAS number 675-09-2, is a cyclic organic compound characterized by its unique structure and properties. It is derived from mesitene, which is a dimethyl-substituted derivative of toluene. Mesitene lactone typically exhibits a colorless to pale yellow appearance and has a distinctive aromatic odor. The compound is known for its relatively low volatility and moderate solubility in organic solvents, making it useful in various chemical applications. Its molecular structure includes a lactone functional group, which contributes to its reactivity and potential applications in organic synthesis. Mesitene lactone is often studied for its role in the synthesis of more complex molecules and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Overall, mesitene lactone is a valuable compound in the field of organic chemistry, with diverse applications based on its chemical properties.

Formula: C₇H₈O₂

InChI: InChI=1S/C7H8O2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3

InChI key: InChIKey=IXYLIUKQQQXXON-UHFFFAOYSA-N

SMILES: CC=1C=C(C)OC(=O)C1

Synonyms:

• 2,4-Dimethyl-α-pyrone
• 2H-Pyran-2-one, 4,6-dimethyl-
• 4,6-Dimethyl-2-pyranone
• 4,6-Dimethyl-2-pyrone
• 4,6-Dimethyl-α-pyrone
• 4,6-Dimethylpyran-2-one
• Mesitene lactone
• NSC 402790
• Sorbic acid, 5-hydroxy-3-methyl-, δ-lactone
• 4,6-Dimethyl-2H-pyran-2-one

4,6-Dimethyl-2H-pyran-2-one

CAS: 675-09-2

Formula: C₇H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 124.1372

Ref: IN-DA003KJQ

4,6-Dimethyl-α-pyrone

CAS: 675-09-2

Formula: C₇H₈O₂

Molecular weight: 124.14

Ref: 7W-GL3406

4,6-Dimethyl-2-pyrone

CAS: 675-09-2

Formula: C₇H₈O₂

Purity: 98%(GC-MS);RG

Color and Shape: Solid

Molecular weight: 124.139

Ref: 10-F045789

4,6-Dimethyl-2-pyrone

CAS: 675-09-2

4,6-Dimethyl-2-pyrone is a hydrogenated aromatic compound that is hydrophobic and has a tannin structure. The compound can be found in plants such as the leaves of the oak tree, where it occurs in small quantities. Tannins are used by plants to protect their cells from damage caused by ultraviolet radiation. 4,6-Dimethyl-2-pyrone is also found in ligands such as organocuprates, which are organic compounds that bind metals such as copper and chromium. It is formed by equilibration of hexadecanoic acid with 2-hydroxyacetophenone via an aluminium chloride catalyst. This reaction mechanism has been shown to be effective at temperatures below 160°C and at pressures of less than 1 bar. 4,6-Dimethyl-2-pyrone can also react with n-hexane to produce 6,6'-dimethylbiphenylsulfonium chloride (

Formula: C₇H₈O₂

Purity: Min. 95%

Molecular weight: 124.14 g/mol

Ref: 3D-FD146325