108-83-8 | 2,6-Dimethyl-4-Heptanone

Packsize	Purity	Availability	Price	Discounted Price
5g	90%	in stock	$26.00	$18.00
25g	90%	in stock	$42.00	$30.00
100g	90%	in stock	$90.00	$63.00
500g	90%	in stock	$251.00	$176.00

Description

• Catalog Number: AB43721
• Chemical Name: 2,6-Dimethyl-4-Heptanone
• CAS Number: 108-83-8
• Molecular Formula: C9H18O
• Molecular Weight: 142.2386
• MDL Number: MFCD00008940
• SMILES: CC(CC(=O)CC(C)C)C

Upstream Synthesis Route

As a professional chemist, I can tell you that 2,6-Dimethyl-4-heptanone, also known as diisobutyl ketone, plays a crucial role in chemical synthesis processes. This compound is commonly employed as a solvent in various chemical reactions and processes due to its unique properties. The presence of the methyl groups at the 2 and 6 positions on the heptanone backbone provides steric hindrance which makes it a valuable reagent in different synthetic pathways.In chemical synthesis, 2,6-Dimethyl-4-heptanone serves as a versatile solvent for reactions that require controlled conditions and precise regulation of temperature. Its excellent solvency properties enable it to dissolve a wide range of organic compounds, making it a popular choice in organic chemistry laboratories. This compound is particularly useful in processes such as Grignard reactions, aldol condensations, and other transformations that involve sensitive substrates.Moreover, 2,6-Dimethyl-4-heptanone can also act as a reactant in certain synthetic routes, participating in reactions to introduce functional groups or modify chemical structures. Its selective reactivity and compatibility with various functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.In summary, the application of 2,6-Dimethyl-4-heptanone in chemical synthesis is instrumental in facilitating numerous reactions by providing a reliable solvent and participating in specific transformations to yield desired products. Its role in enabling controlled, efficient, and selective synthesis processes highlights its significance in the realm of organic chemistry.