Interesting facts
              Interesting Facts About 6-Methylheptan-2-one
6-Methylheptan-2-one, an intriguing ketone, belongs to the class of organic compounds known for their distinct carbonyl group. This compound showcases a unique structure that contributes to its diverse applications in chemistry and industry.
Key Features
- Functional Group: As a ketone, it features a carbonyl group (C=O) situated in the molecule, specifically between the carbon chain, which notably influences its reactivity and properties.
- Branching: The presence of a methyl group on the sixth carbon atom adds branching to its structure, which can affect the compound's volatility and physical characteristics.
- Applications: This compound is commonly utilized as an industrial solvent and is valuable in the synthesis of other chemical compounds within the fragrance and flavor industries.
Chemical Behavior
6-Methylheptan-2-one exhibits interesting reactivity patterns typical of ketones. It can undergo several types of chemical reactions, including:
- Nucleophilic Addition: The carbonyl group is susceptible to nucleophiles, making it a target for various chemical reactions including synthesis.
- Oxidation-Reaction: Ketones can participate in oxidation reactions, yielding carboxylic acids or further transformations under certain conditions.
- Condensation Reactions: It can also engage in condensation reactions, producing larger organic molecules that are significant in organic synthesis.
Fun Facts
- 6-Methylheptan-2-one has been studied for its odor profile, leading to its use in developing synthetic fragrances.
- This compound is a part of the wider family of aliphatic ketones, essential for creating various specialty chemicals.
In summary, 6-Methylheptan-2-one is not just a simple organic molecule; it acts as a versatile building block in chemical synthesis and has various industrial applications, making it an essential item within the study of organic chemistry.
Synonyms
          6-Methylheptan-2-one
          6-METHYL-2-HEPTANONE
          928-68-7
          2-Heptanone, 6-methyl-
          2-Isooctanone
          2-Methyl-6-heptanone
          Methyl isohexyl ketone
          N203Q7UI56
          ISOOCTAN-2-ONE
          EINECS 213-179-7
          NSC 39665
          NSC-39665
          DTXSID7061302
          DPLGXGDPPMLJHN-UHFFFAOYSA-
          Methylheptanon
          2Methyl6heptanone
          6Methylheptan2one
          2Heptanone, 6methyl
          DTXCID3048819
          213-179-7
          inchi=1/c8h16o/c1-7(2)5-4-6-8(3)9/h7h,4-6h2,1-3h3
          6-methyl-heptan-2-one
          MFCD00026527
          Methyl 4-Methylpentyl Ketone
          2-Heptanone,6-methyl-
          UNII-N203Q7UI56
          2-Isooctanone; 2-Methyl-6-heptanone; 6-Methyl-2-heptanone; Isooctan-2-one; Methyl isohexyl ketone; NSC 39665
          NSC39665
          6-Methyl 2-heptanone
          6-METHYLHEPTANONE
          SCHEMBL130602
          CHEBI:184396
          6-Methyl-2-heptanone, AldrichCPR
          AAA92868
          LMFA12000041
          AKOS009157571
          BS-17861
          SY052020
          DB-242815
          CS-0154232
          M0700
          NS00021391
          EN300-72298
          D81757
          Q27284399
              
Solubility of 6-methylheptan-2-one
6-methylheptan-2-one, with the chemical formula C8H16O, is a ketone compound that displays interesting solubility characteristics. As a medium-chain organic molecule, its solubility can be influenced by several factors:
In summary, while 6-methylheptan-2-one has some degree of solubility in water due to its polar carbonyl group, it is predominantly soluble in nonpolar and polar organic solvents. This characteristic division in solubility behavior highlights the significance of molecular structure in determining the interactions potential with different types of solvents.