CAS 42348-86-7
:5-Chloro-1-indanone
Description:
5-Chloro-1-indanone is an organic compound characterized by its indanone structure, which features a fused benzene and cyclopentanone ring system. The presence of a chlorine atom at the 5-position of the indanone ring contributes to its reactivity and potential applications in organic synthesis. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound exhibits moderate solubility in organic solvents, while its solubility in water is limited. 5-Chloro-1-indanone may undergo typical reactions associated with carbonyl compounds, such as nucleophilic addition and condensation reactions. Safety data indicates that, like many chlorinated compounds, it should be handled with care due to potential toxicity and environmental concerns. Proper storage and handling protocols are essential to ensure safety in laboratory and industrial settings.
Formula:C9H7ClO
InChI:InChI=1S/C9H7ClO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2
InChI key:InChIKey=MEDSHTHCZIOVPU-UHFFFAOYSA-N
SMILES:O=C1C=2C(CC1)=CC(Cl)=CC2
Synonyms:- 1-Indanone, 5-chloro-
- 1H-Inden-1-one, 5-chloro-2,3-dihydro-
- 5-Chloro Indanone
- 5-Chloro-1-indanone,99%
- 5-Chloro-2,3-Dihydroinden-1-One
- 5-Chloro-2,3-dihydro-1H-inden-1-one
- 5-Chloroindan-1-Indanone
- 5-Chloroindan-1-One
- 5-Chloro-1-indanone
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5-Chloro-1-indanone
CAS:Formula:C9H7ClOPurity:>97.0%(GC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:166.605-Chloroindan-1-one
CAS:5-Chloroindan-1-oneFormula:C9H7ClOPurity:≥95%Color and Shape:off-white to pale yellow. Solid-CrystalsMolecular weight:166.604275-Chloro-1-Indanone
CAS:Controlled ProductApplications 5-Chloro-1-Indanone is used as a reagent in the synthesis of novel tricyclic pyrazoles as CB1 and CB2 cannabinoid receptors. Also used in he synthesis of heteroarylmethylidene cubstituted compounds as selective inhibitors of aldosterone synthase.
References Ulmschneider, S. et al.: J. Med. Chem., 48, 1563 (2005); Ulmschneider, S. et al.: J. Med. Chem., 48, 1563 (2005);Formula:C9H7ClOColor and Shape:NeatMolecular weight:166.65-Chloro-1-indanone
CAS:5-Chloro-1-indanone is an organic molecule with a reactive functional group that can react with other molecules. The most common reaction is the Friedel-Crafts reaction, which is used to make alkenes from aldehydes and aluminum chloride. 5-Chloro-1-indanone is also used in the acylation reaction, which involves the transfer of an acyl group to a molecule. This process has many applications, such as synthesis of pesticides and pharmaceuticals, and can be used to produce low energy chlorine gas. Panc-1 cells are often used in anticancer research because they are sensitive to carcinogens. 5-Chloro-1-indanone was shown to inhibit cell growth in these cells by reacting with hydrogen chloride (HCl) in water to form 5-(chloromethyl)-1H indene and hydrochloric acid (HCl).Formula:C9H7ClOPurity:Min. 95%Color and Shape:PowderMolecular weight:166.6 g/mol
