CAS 5682-75-7
:3-chlorocyclohex-2-en-1-one
Description:
3-Chlorocyclohex-2-en-1-one is an organic compound characterized by its cyclohexene structure with a ketone functional group and a chlorine substituent. It features a six-membered carbon ring with a double bond between the second and third carbon atoms, and a carbonyl group (C=O) at the first position. The presence of the chlorine atom at the third carbon introduces unique reactivity and influences the compound's physical and chemical properties. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and may exhibit moderate stability under standard conditions. 3-Chlorocyclohex-2-en-1-one can participate in various chemical reactions, including nucleophilic additions and substitutions, making it of interest in synthetic organic chemistry. Its applications may extend to the synthesis of more complex molecules, pharmaceuticals, or agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health hazards if inhaled or ingested.
Formula:C6H7ClO
InChI:InChI=1/C6H7ClO/c7-5-2-1-3-6(8)4-5/h4H,1-3H2
SMILES:C1CC(=CC(=O)C1)Cl
Synonyms:- 2-Cyclohexen-1-One, 3-Chloro-
- 3-Chloro-2-cyclohexen-1-one
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Found 3 products.
3-Chlorocyclohex-2-enone
CAS:<p>3-Chlorocyclohex-2-enone</p>Purity:95%Color and Shape:SolidMolecular weight:130.57g/mol3-chlorocyclohex-2-en-1-one
CAS:<p>3-Chlorocyclohex-2-en-1-one is an organic compound that is a member of the class of compounds called alkylating agents. It can be synthesized by reacting piperidine with an aryl chloride in the presence of phosphine. 3-Chlorocyclohex-2-en-1-one reacts with dimethylformamide to produce aziridines that are used as ligands in catalysis. The reaction rate of 3-chlorocyclohex-2-en-1-one is dependent on the concentration of nucleophile and electrophile, and it can be described by kinetics and kinetics.</p>Formula:C6H7ClOPurity:Min. 95%Molecular weight:130.58 g/mol
