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Thermo Scientific Chemicals
2-Chlorophenyl cyclopentyl ketone, 97%
CAS: 6740-85-8 | C12H13ClO | 208.685 g/mol
化学物質識別子
CAS6740-85-8
IUPAC Name(2-chlorophenyl)(cyclopentyl)methanone
Molecular FormulaC12H13ClO
InChI KeyQIJMMRNZBJHXRI-UHFFFAOYSA-N
SMILESClC1=CC=CC=C1C(=O)C1CCCC1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear, colourless to yellow
Formliquid
Refractive Index1.5445-1.5495 @20?C
Assay (GC)>96.0%
2-Chlorophenyl cyclopentyl ketone is used as a reagent in the preparation of bicyclic and polycyclic aromatic hydrocarbons. It acts as a pharmaceutical intermediate and also as an intermediate of ketamine.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Chlorophenyl cyclopentyl ketone is used as a reagent in the preparation of bicyclic and polycyclic aromatic hydrocarbons. It acts as a pharmaceutical intermediate and also as an intermediate of ketamine.
Solubility
Slightly miscible with chloroform and ethyl acetate.
Notes
Incompatible with oxidizing agents.
2-Chlorophenyl cyclopentyl ketone is used as a reagent in the preparation of bicyclic and polycyclic aromatic hydrocarbons. It acts as a pharmaceutical intermediate and also as an intermediate of ketamine.
Solubility
Slightly miscible with chloroform and ethyl acetate.
Notes
Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Li, Y.; Coller, J. K.; Hutchinson, M. R.; Klein, K.; Zanger, U. M.; Stanley, N. J.; Abell, A. D.; Somogyi, A. A. The CYP2B6* 6 allele significantly alters the N-demethylation of ketamine enantiomers in vitro. Drug Metab. Dispos. 2013, 41 (6), 1264-1272.
- Jose, J.; Gamage, S. A.; Harvey, M. G.; Voss, L. J.; Sleigh, J. W.; Denny, W. A. Structure-activity relationships for ketamine esters as short-acting anaesthetics. Bioorg. Med. Chem. 2013, 21 (17), 5098-5106.