CAS 40926-77-0
:Acetyl chloride, (2-naphthalenyloxy)-
Description:
Acetyl chloride, (2-naphthalenyloxy)-, with the CAS number 40926-77-0, is an organic compound characterized by its acetyl chloride functional group attached to a 2-naphthalenyloxy moiety. This compound typically appears as a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity and volatility. It is known for its role as an acylating agent in organic synthesis, particularly in the formation of esters and amides. The presence of the naphthalenyloxy group enhances its reactivity, allowing it to participate in various chemical reactions, including nucleophilic substitutions. Acetyl chloride is sensitive to moisture and can hydrolyze to form acetic acid, making it necessary to handle it under anhydrous conditions. Additionally, it is classified as a corrosive substance, requiring appropriate safety measures during handling and storage. Overall, this compound is valuable in synthetic organic chemistry, particularly in the preparation of complex molecules and intermediates.
Formula:C12H9ClO2
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Found 3 products.
(2-Naphthyloxy)acetyl Chloride
CAS:Controlled Product<p>Applications (2-Naphthyloxy)acetyl Chloride serves as one of the reagents for the discovery of indoline-2-carboxamide derivatives as new classs of brain-penetrant inhibitors of trypanosoma brucei. Also in preparation and antibacterial activity of N-(phenylquinazolinonyl) aryl-amides by amidation of amino(phenyl)quinazolone with aroyl chlorides<br>References Cleghorn, L. A., et al.: J. Med. Chem., 58, 7695 (2015); Prajapati, A. K., et al.: Indian J. Heterocycl. Chem., 19, 269 (2010)<br></p>Formula:C12H9ClO2Color and Shape:NeatMolecular weight:220.652(2-Naphthyloxy)acetyl chloride
CAS:<p>(2-Naphthyloxy)acetyl chloride is an inhibitor of alcohol dehydrogenase, which is the enzyme that catalyzes the conversion of ethanol to acetaldehyde. It has been shown to be active against grapevine, but not against the yeast Saccharomyces cerevisiae. (2-Naphthyloxy)acetyl chloride inhibits alcohol dehydrogenase with a potency comparable to hexanol and ethylene glycol. It also inhibits esterases, which may account for its inhibitory effect on vinifera l. (2-Naphthyloxy)acetyl chloride has been shown to be more selective in inhibiting both alcohol and aldehyde dehydrogenases than hexanol or ethylene glycol.</p>Formula:C12H9ClO2Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:220.65 g/mol
