CAS 2040-20-2
:1-(4-methoxyphenyl)-2-methylpropan-1-one
Description:
1-(4-Methoxyphenyl)-2-methylpropan-1-one, also known as p-methoxyphenyl isobutyl ketone, is an organic compound characterized by its ketone functional group. It features a propanone backbone with a methoxy group (-OCH3) attached to a phenyl ring at the para position, along with a methyl group on the second carbon of the propanone chain. This compound is typically a colorless to pale yellow liquid with a sweet, aromatic odor. It is soluble in organic solvents and has limited solubility in water. The presence of the methoxy group enhances its lipophilicity, making it useful in various applications, including as a fragrance component and in the synthesis of other organic compounds. Additionally, it may exhibit biological activity, which has led to interest in its potential use in pharmaceuticals and as a research chemical. Safety precautions should be taken when handling this substance, as it may pose health risks if inhaled or ingested.
Formula:C11H14O2
InChI:InChI=1/C11H14O2/c1-8(2)11(12)9-4-6-10(13-3)7-5-9/h4-8H,1-3H3
SMILES:CC(C)C(=O)c1ccc(cc1)OC
Synonyms:- 1-Propanone, 1- (4-methoxyphenyl)-2-methyl-
- 4'-Methoxy-2-methylpropiophenone
- Isopropyl 4-methoxyphenyl ketone
- Isopropyl p-methoxyphenyl ketone
- p-Methoxyisobutyrophenone
- Propiophenone, 4'-methoxy-2-methyl-
- 1-(4-Methoxyphenyl)-2-methylpropan-1-one
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
1-(4-Methoxyphenyl)-2-methylpropan-1-one
CAS:Formula:C11H14O2Purity:97%Color and Shape:LiquidMolecular weight:178.22771-(4-Methoxyphenyl)-2-methylpropan-1-one
CAS:<p>1-(4-Methoxyphenyl)-2-methylpropan-1-one is an organic compound with the chemical formula CH3COCH(OCH2CH3). It is a colorless liquid that is soluble in water, ether, and most organic solvents. It has a boiling point of 154 °C at 1 atm and its density is 0.921 g/mL at 25 °C. This compound can be used as an alkylating agent for aromatic compounds, acyl halides, carbonyls, and other reactive groups. The reaction mechanism for this compound begins with a nucleophilic attack on the electrophilic carbon atom by the oxygen atom of the methoxy group to form an acetal intermediate. The intermediate then undergoes hydrolysis to form a new c–h bond and a methyl ether product.</p>Formula:C11H14O2Purity:Min. 95%Molecular weight:178.23 g/mol

