CAS 766-66-5
:2-Chlorocycloheptanone
Description:
2-Chlorocycloheptanone is a cyclic ketone characterized by the presence of a seven-membered carbon ring with a ketone functional group and a chlorine substituent at the second carbon position. Its molecular formula is C7H11ClO, indicating it contains seven carbon atoms, eleven hydrogen atoms, one chlorine atom, and one oxygen atom. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is moderately soluble in organic solvents and exhibits limited solubility in water due to its hydrophobic cycloalkane structure. 2-Chlorocycloheptanone is used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the ketone and chlorine functional groups, allowing for various chemical transformations. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective equipment should be used to minimize exposure.
Formula:C7H11ClO
InChI:InChI=1S/C7H11ClO/c8-6-4-2-1-3-5-7(6)9/h6H,1-5H2
InChI key:InChIKey=SDSZGDVXUFWFAA-UHFFFAOYSA-N
SMILES:ClC1C(=O)CCCCC1
Synonyms:- 2-Chlorocycloheptanone
- Brn 1099282
- Cycloheptanone, 2-chloro-
- alpha-Chlorocycloheptanone
- 2-Chlorocycloheptan-1-one
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
2-Chlorocycloheptanone
CAS:<p>2-Chlorocycloheptanone is a quaternary ammonium salt that has a cyclic and conformational geometry. It reacts with sodium borohydride to form the corresponding tertiary alcohol, and it can be reduced by borohydride or carbon tetrachloride to form the corresponding secondary alcohol. The compound is used in the synthesis of enamines and piperazinil esters, which are used in the field of population genetics. 2-Chlorocycloheptanone has been shown to yield high yields of product when synthesized from cyclohexanol.</p>Formula:C7H11ClOPurity:Min. 95%Molecular weight:146.61 g/mol
