CAS 470-49-5
:Pentanoicacid, 2,2-dimethyl-4-oxo-
Description:
Pentanoic acid, 2,2-dimethyl-4-oxo- (CAS 470-49-5) is an organic compound characterized by its carboxylic acid functional group and a ketone group. It features a five-carbon chain (pentanoic acid) with two methyl groups attached to the second carbon and a ketone group at the fourth carbon. This structure contributes to its unique chemical properties, including its ability to participate in various chemical reactions typical of carboxylic acids and ketones. The presence of the carboxylic acid group imparts acidic characteristics, allowing it to donate protons in solution, while the ketone group can engage in nucleophilic addition reactions. The compound is typically a colorless liquid or solid at room temperature and may have a characteristic odor. Its solubility in water is moderate, influenced by the length of the carbon chain and the functional groups present. Pentanoic acid derivatives are often utilized in organic synthesis, pharmaceuticals, and as intermediates in various chemical processes.
Formula:C7H12O3
Synonyms:- 2,2-Dimethyl-4-oxopentanoic acid
- Mesitonic acid (6CI)
- 2,2-Dimethyllevulinic acid
- Levulinicacid, 2,2-dimethyl- (7CI,8CI)
- a,a-Dimethyllevulinicacid
- Pentanoic acid, 2,2-dimethyl-4-oxo-
- mesitonic acid
- α,α-dimethyllevulinic acid
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Found 1 products.
2,2-Dimethyl-4-oxopentanoic acid
CAS:<p>2,2-Dimethyl-4-oxopentanoic acid is a molecule that belongs to the group of polarizers. It has an important role in the nervous system and has been shown to be involved in numerous diseases such as psychotic disorders, diabetes mellitus, and inflammatory diseases. 2,2-Dimethyl-4-oxopentanoic acid is synthesized from two molecules of acetyl coenzyme A via a series of reactions. In addition, this molecule is hydrolyzed by phospholipase C to form diacylglycerol. 2,2-Dimethyl-4-oxopentanoic acid also inhibits the production of inflammatory cytokines such as IL-1β and TNFα.</p>Formula:C7H12O3Purity:Min. 95%Molecular weight:144.17 g/mol
