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Methyl 6-oxohexanoate
CAS: 6654-36-0
Ref. 3D-FM25462
1g | To inquire | ||
2g | To inquire | ||
5g | To inquire | ||
10g | To inquire | ||
500mg | To inquire |
Product Information
- Adipic semialdehyde methyl ester5-Carbomethoxy-1-pentanal5-Formylpentanoic acid methyl ester
- 5-Carbomethoxy-1-pentanal
- 5-Formylpentanoic acid, methyl ester
- 5-Formylvaleric acid, methyl ester
- 6-Oxohexanoic acid methyl ester
- Adipaldehydic acid, methyl ester
- Adipic acid semialdehyde methyl ester
- Hexanoic acid, 6-oxo-, methyl ester
- Methyl 5-formylpentanoate
- Methyl 5-formylvalerate
- See more synonyms
- Methyl 6-oxocaproate
- Methyl adipaldehydate
Methyl 6-oxohexanoate is a synthetic molecule that is structurally related to nigrum. It has been shown to be hydrolyzed by the enzyme β-oxidation process, which converts methyl 6-oxohexanoate into fatty acids and ketones. Methyl 6-oxohexanoate can also undergo a series of reactions in which it reacts with an ozone molecule, forming ozonides. The geometric isomers of methyl 6-oxohexanoate are also known as cis and trans forms, which differ in their physical properties due to the orientation of their hydroxyl group on the double bond. The cis form is more stable than the trans form because it has less steric hindrance from neighboring groups. Deuteration occurs when hydrogen atoms are replaced with deuterium, which can be accomplished by reacting methyl 6-oxohexanoate with piperonyl butoxide and thioacetal in a reaction catalyzed by am
Chemical properties
Technical inquiry about: 3D-FM25462 Methyl 6-oxohexanoate
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