CAS 16807-60-6
:3-Methoxy-2-cyclohexen-1-one
Description:
3-Methoxy-2-cyclohexen-1-one is an organic compound characterized by its unique structure, which includes a methoxy group (-OCH3) and a cyclohexenone moiety. This compound features a six-membered cyclohexene ring with a double bond and a carbonyl group (C=O) that contributes to its reactivity and potential applications in organic synthesis. The presence of the methoxy group enhances its solubility in organic solvents and can influence its reactivity, making it a useful intermediate in various chemical reactions. 3-Methoxy-2-cyclohexen-1-one may exhibit interesting biological activities, which can be explored for potential pharmaceutical applications. Its molecular structure allows for various functionalization possibilities, making it a valuable compound in synthetic organic chemistry. Additionally, the compound's stability and reactivity can be influenced by factors such as temperature and the presence of other reagents, which are important considerations in laboratory settings. Overall, 3-Methoxy-2-cyclohexen-1-one is a versatile compound with significant implications in both research and industrial applications.
Formula:C7H10O2
InChI:InChI=1/C7H10O2/c1-9-7-4-2-3-6(8)5-7/h5H,2-4H2,1H3
InChI key:InChIKey=JFTPIEHHCQPVCS-UHFFFAOYSA-N
SMILES:O(C)C1=CC(=O)CCC1
Synonyms:- 2-Cyclohexen-1-one, 3-methoxy-
- 3-Methoxy-2-Cyclohexen-1-One 99+%
- 3-Methoxy-2-cyclohexenone
- 3-Methoxycyclohex-2-En-1-One
- 3-Methoxy-2-cyclohexen-1-one
- 3-Methoxycyclohex-2-enone
- 3-METHOXY-2-CYCLOHEXEN-1-ONE FOR SYNTHES
- Einecs 240-837-0
- 3-METH0XYCYCL0HEX-2-EN0NE
- 1-Methoxycyclohexene-3-one
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Found 4 products.
2-Cyclohexen-1-one, 3-methoxy-
CAS:Formula:C7H10O2Purity:96%Color and Shape:SolidMolecular weight:126.15313-Methoxy-2-cyclohexen-1-one
CAS:<p>3-Methoxy-2-cyclohexen-1-one is a stereoisomer of cyclohexanone. It is the product of an asymmetric synthesis by irradiation. The reaction requires methoxyphenol and acetyl chloride, with isomers being separated by gel chromatography. The stereoselectivity of the reaction has been shown to be high, with the desired product being oriented in a chiral environment. A hydrochloric acid solution is used to convert 3-methoxy-2-cyclohexen-1-one into 2,3-dimethoxybenzoic acid.</p>Formula:C7H10O2Purity:Min. 95%Molecular weight:126.15 g/mol



