4500-47-4

Basic information

• Product Name: 2-Butanone, 3-(3-methoxyphenyl)-
• CAS NO: 4500-47-4
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 4500-47-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Butanone, 3-(3-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butanone, 3-(3-methoxyphenyl)-(4500-47-4)
• EPA Substance Registry System: 2-Butanone, 3-(3-methoxyphenyl)-(4500-47-4)

Safety Data

• Hazardous Substances Data: 4500-47-4(Hazardous Substances Data)

Usage

General Description

2-Butanone, 3-(3-methoxyphenyl)- is a chemical compound with the molecular formula C11H14O2. It is also known as Methyl ethyl ketone, 3-(3-methoxyphenyl)- or MEK-3-(3-methoxyphenyl). 2-Butanone, 3-(3-methoxyphenyl)- is an aromatic ketone with a methoxy group on the third carbon of the phenyl ring. It is commonly used as a solvent in various industrial processes, including the production of plastics, textiles, and pharmaceuticals. Additionally, it can be found in some consumer products such as paints, adhesives, and coatings. This chemical is flammable and should be handled with care in a well-ventilated area.

Upstream product

• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 5912-89-0 2-methyl-1-(3-methoxyphenyl)propene 
• 3027-13-2 1-(3-methoxyphenyl)propan-2-one 
• 74-88-4 methyl iodide 
• 1798-09-0 m-methoxyphenylacetic acid 
• 591-31-1 3-methoxy-benzaldehyde 
• 18738-95-9 1-(m-methoxyphenyl)-2-nitro-1-propene 

Downstream Products

• 1256242-27-9 (S)-3-(3-methoxylphenyl)butan-2-one 
• 1173092-36-8 (R)-3-(3-methoxylphenyl)butan-2-one 
• 93351-40-7 (+/-)-1-(3-methoxyphenyl)ethyl acetate 
• 120125-64-6 3-(m-methoxyphenyl)butan-2-ol 
• 195001-55-9 3-methoxy-6-(3'-methoxyphenyl)-6-methylcyclohex-2-enone 
• 170753-17-0 4-(3'-methoxyphenyl)-4-methyl-3-vinylcyclohex-2-enone 
• 21894-68-8 2-(m-Methoxyphenyl)-3-butylamin 

Relevant articles and documents

Synthesis of Functionalized Dihydrobenzofurans by Direct Aryl C?O Bond Formation under Mild Conditions

A method for the synthesis of dihydrobenzofurans by a direct aryl C?O bond formation is described. A mechanistic pathway for the reaction, distinct from previously described similar transformations, allows for mild reaction conditions that are expected to be compatible with functionalized substrates.

Use of conjugated dienones in cyclialkylations: Total syntheses of arucadiol, 1,2-didehydromiltirone, (±)-hinokione, (±)-nimbidiol, sageone, and miltirone

Functionalized hydrophenanthrenes can be prepared using a cyclialkylation-based strategy. These annulations are highly dependent on the directing effects of the arene substitutents and on conformational considerations. The utility of this methodology was featured in the syntheses of six diterpenoids.