CAS 106967-74-2
:2-(3-Methoxyphenoxy)acetyl chloride
Description:
2-(3-Methoxyphenoxy)acetyl chloride, with the CAS number 106967-74-2, is an organic compound characterized by its acetyl chloride functional group and a methoxy-substituted phenoxy moiety. This compound typically appears as a colorless to pale yellow liquid and is known for its reactivity, particularly in acylation reactions. The presence of the acetyl chloride group makes it a potent acylating agent, allowing it to react with various nucleophiles, including alcohols and amines, to form esters and amides, respectively. The methoxy group enhances the compound's solubility in organic solvents and may influence its reactivity and stability. Additionally, this compound is often utilized in organic synthesis and pharmaceutical applications, where it serves as an intermediate in the preparation of more complex molecules. Due to its reactive nature, it should be handled with care, as it can release hydrochloric acid upon hydrolysis, posing potential hazards. Proper safety measures and protocols should be followed when working with this substance in a laboratory setting.
Formula:C9H9ClO3
InChI:InChI=1S/C9H9ClO3/c1-12-7-3-2-4-8(5-7)13-6-9(10)11/h2-5H,6H2,1H3
InChI key:InChIKey=TVVBVERHHKVWFG-UHFFFAOYSA-N
SMILES:O(CC(Cl)=O)C1=CC(OC)=CC=C1
Synonyms:- (3-Methoxy-phenoxy)-acetyl chloride
- Acetyl chloride, (3-methoxyphenoxy)-
- Acetyl chloride, 2-(3-methoxyphenoxy)-
- 2-(3-Methoxyphenoxy)acetyl chloride
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