CAS 13494-07-0

3,5-Dimethyl-1,2-cyclopentanedione

Description:

3,5-Dimethyl-1,2-cyclopentanedione, with the CAS number 13494-07-0, is an organic compound characterized by its cyclic structure and the presence of two ketone functional groups. This compound features a cyclopentane ring with two methyl groups attached at the 3 and 5 positions, and two carbonyl groups at the 1 and 2 positions, which contribute to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the diketone functionality allows for various chemical reactions, including condensation and oxidation, making it useful in the synthesis of more complex organic molecules. Additionally, its structural features may impart interesting properties such as solubility in organic solvents and potential biological activity. As with many diketones, it may exhibit tautomerism, leading to different structural forms in solution. Safety data should be consulted for handling and storage, as it may pose health risks if not managed properly.

Formula: C₇H₁₀O₂

InChI: InChI=1S/C7H10O2/c1-4-3-5(2)7(9)6(4)8/h4-5H,3H2,1-2H3

InChI key: InChIKey=MIDXCONKKJTLDX-UHFFFAOYSA-N

SMILES: O=C1C(=O)C(C)CC1C

Synonyms:

• 3,5-Dimethyl-1,2-cyclopentanedione
• Coronol
• 1,2-Cyclopentanedione, 3,5-dimethyl-

3,5-Dimethyl-1,2-Cyclopentanedione

CAS: 13494-07-0

Formula: C₇H₁₀O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 126.1531

Ref: IN-DA003IOA

3,5-Dimethylcyclopentane-1,2-dione

CAS: 13494-07-0

3,5-Dimethylcyclopentane-1,2-dione

Purity: 98+%

Molecular weight: 126.15g/mol

Ref: 54-OR80556

3,5-Dimethylcyclopentane-1,2-dione

CAS: 13494-07-0

Purity: 98%

Molecular weight: 126.1549988

Ref: 10-F655971

3,5-Dimethyl-1,2-cyclopentadione

CAS: 13494-07-0

3,5-Dimethyl-1,2-cyclopentadione (DMC) is a natural compound that belongs to the group of cyclopentadione compounds. It is used in analytical chemistry for the determination of 3,5-dimethyl-1,2-dihydropyridinium ion (DMP). The structural analysis of DMC has been shown with synchronous fluorescence. This method can be used to detect cancer cells in human tissue samples. DMC was also found to be toxic to diabetic patients when administered orally at a concentration of 10 mM. The toxicity study showed that this compound causes severe hepatotoxicity and kidney damage. Whole genome sequencing and dietary studies were performed by the researchers to investigate the cause of an outbreak of diarrhea among school children in Japan. Sodium hydroxide solution was used as a sample preparation agent in these studies. Glycosidic bonds are found in many natural products such as DMC and are important for binding water molecules

Formula: C₇H₁₀O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 126.15 g/mol

Ref: 3D-NAA49407