1131-62-0 | 1-(3,4-Dimethoxyphenyl)ethanone

Packsize	Purity	Availability	Price	Discounted Price
25g	97%	in stock	$13.00	$9.00
100g	97%	in stock	$43.00	$30.00
5kg	97%	in stock	$1,879.00	$1,316.00

Description

• Catalog Number: AB63743
• Chemical Name: 1-(3,4-Dimethoxyphenyl)ethanone
• CAS Number: 1131-62-0
• Molecular Formula: C10H12O3
• Molecular Weight: 180.2005
• MDL Number: MFCD00008737
• SMILES: COc1cc(ccc1OC)C(=O)C

Computed Properties

• Complexity: 179
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• XLogP3: 1.8

Upstream Synthesis Route

1-(3,4-Dimethoxyphenyl)ethanone, also known as DMEK, is a versatile compound widely utilized in chemical synthesis for various applications. With its unique structure, this compound plays a crucial role in the production of pharmaceuticals, fragrances, and other organic compounds.In chemical synthesis, 1-(3,4-Dimethoxyphenyl)ethanone acts as a key intermediate in the creation of functionalized molecules and organic building blocks. Its efficient reactivity and compatibility with a wide range of reagents make it an ideal precursor for the synthesis of diverse chemical compounds. This compound is commonly used in the construction of complex molecules through processes such as acylation, alkylation, and condensation reactions.Furthermore, 1-(3,4-Dimethoxyphenyl)ethanone can be employed in the synthesis of natural products, pharmaceuticals, and fine chemicals. Its presence in the chemical synthesis industry facilitates the development of new drug candidates, flavors, and fragrances. The ability of this compound to undergo various transformations under controlled conditions makes it a valuable asset in the creation of novel chemical entities.Overall, the application of 1-(3,4-Dimethoxyphenyl)ethanone in chemical synthesis highlights its significance in advancing research and innovation within the field of organic chemistry. This versatile compound continues to be a staple in the toolbox of synthetic chemists worldwide, contributing to the synthesis of diverse compounds with valuable properties and potential applications.

Literature

• Neuroprotective compounds isolated from Cynanchum paniculatum.

  Archives of pharmacal research 20120301

• (E)-1-(3,4-Dimeth-oxy-phen-yl)-3-[4-(methyl-sulfan-yl)phen-yl]prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20110901

• (E)-3-(2,4-Dimeth-oxy-phen-yl)-1-(3,4-dimeth-oxy-phen-yl)prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20101101

• Design, synthesis, and biological activity of novel 4-(3,4-dimethoxyphenyl)-2-methylthiazole-5-carboxylic acid derivatives.

  Bioorganic & medicinal chemistry 20040601