CAS 4629-80-5
:1,3-Dimethyl-4-piperidone
Description:
1,3-Dimethyl-4-piperidone, with the CAS number 4629-80-5, is an organic compound belonging to the piperidone class. It features a six-membered piperidine ring with two methyl groups attached at the 1 and 3 positions and a ketone functional group at the 4 position. This compound is typically a colorless to pale yellow liquid with a characteristic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. 1,3-Dimethyl-4-piperidone is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It exhibits moderate toxicity and should be handled with care, following appropriate safety protocols. The compound can undergo various chemical reactions, including nucleophilic addition and condensation, making it versatile in organic synthesis. Its structural features contribute to its reactivity and potential applications in medicinal chemistry and material science.
Formula:C7H13NO
InChI:InChI=1S/C7H13NO/c1-6-5-8(2)4-3-7(6)9/h6H,3-5H2,1-2H3
InChI key:InChIKey=BGDGMIWDPMJYPP-UHFFFAOYSA-N
SMILES:CC1C(=O)CCN(C)C1
Synonyms:- 1,3-Dimethyl-4-Piperidone
- 1,3-Dimethylpiperdone
- 1,3-Dimethylpiperidin-4-one
- 4-Piperidinone, 1,3-dimethyl-
- 4-Piperidone, 1,3-dimethyl-
- 1,3-Dimethyl-4-piperidinone
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Found 6 products.
1,3-dimethylpiperidin-4-one
CAS:Formula:C7H13NOPurity:98%Color and Shape:LiquidMolecular weight:127.18421,3-Dimethylpiperidin-4-one
CAS:1,3-Dimethylpiperidin-4-onePurity:97%Color and Shape:LiquidMolecular weight:127.18g/mol1,3-Dimethyl-4-piperidone
CAS:Formula:C7H13NOPurity:>98.0%(GC)(T)Color and Shape:Colorless to Yellow to Orange clear liquidMolecular weight:127.191,3-Dimethyl-piperidin-4-one
CAS:Formula:C7H13NOPurity:97%Color and Shape:ClearMolecular weight:127.1871,3-Dimethylpiperidin-4-one
CAS:Controlled ProductFormula:C7H13NOColor and Shape:NeatMolecular weight:127.1841,3-Dimethyl-4-piperidone
CAS:<p>1,3-Dimethyl-4-piperidone is a colorless liquid at room temperature that is soluble in water and polar organic solvents. It is a protonated nucleophile that reacts with electrophiles to form alkylations. 1,3-Dimethyl-4-piperidone also reacts with chloride to form an imine, which can be hydrolyzed to yield piperidine. A Grignard reagent can be formed from 1,3-dimethyl-4-piperidone and potassium phosphate. The nature of the product obtained depends on the order of addition of reactants. 1,3-Dimethyl-4-piperidone has been shown to have a number of isomers.</p>Formula:C7H13NOPurity:Min. 95%Molecular weight:127.19 g/mol





