776-99-8 | 3,4-Dimethoxyphenylacetone

Availability
Typically In Stock

Description

• Catalog Number: AC69197
• Chemical Name: 3,4-Dimethoxyphenylacetone
• CAS Number: 776-99-8
• Molecular Formula: C11H14O3
• Molecular Weight: 194.2271
• MDL Number: MFCD00008772
• SMILES: COc1cc(ccc1OC)CC(=O)C
• NSC Number: 16700

Computed Properties

• Complexity: 191
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• XLogP3: 1.1

Upstream Synthesis Route

1-(3,4-Dimethoxyphenyl)propan-2-one, also known as $name$, is a versatile organic compound commonly used in chemical synthesis. With its structure consisting of a propan-2-one backbone attached to a 3,4-dimethoxyphenyl group, this compound offers a range of applications in the field of chemistry.One key application of 1-(3,4-Dimethoxyphenyl)propan-2-one is as a building block in the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure and functional groups make it a valuable intermediate in the production of complex organic compounds. By strategically modifying and functionalizing this compound, chemists can access a wide array of derivatives with diverse properties and activities.Additionally, 1-(3,4-Dimethoxyphenyl)propan-2-one serves as a crucial reagent in the formation of carbon-carbon and carbon-heteroatom bonds. Through reactions such as Grignard additions, aldol condensations, and Friedel-Crafts acylations, this compound can be transformed into more intricate structures, enabling the synthesis of target molecules with specific functionalities and stereochemistries.In summary, the role of 1-(3,4-Dimethoxyphenyl)propan-2-one in chemical synthesis extends beyond a simple starting material, showcasing its importance as a key component in the construction of complex organic molecules with applications in pharmaceuticals, materials science, and other research fields.

Literature

• Microbial synthesis of chiral amines by (R)-specific transamination with Arthrobacter sp. KNK168.

  Applied microbiology and biotechnology 20060101

• Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination.

  Biotechnology letters 20031101