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Assay
99%
form
powder
mp
94-98 °C (lit.)
functional group
chloro
ketone
SMILES string
Clc1ccc2C(=O)CCc2c1
InChI
1S/C9H7ClO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2
InChI key
MEDSHTHCZIOVPU-UHFFFAOYSA-N
General description
5-Chloro-1-indanone is a 5-halo-1-indanone. It participates in the Irie′s synthesis of substituted pyridines. 5-Chloro-1-indanone has a stable triclinic crystal structure and has intermolecular forces of C-H...O, C-H...Π, CO...Cl and Π...Π types.
Application
5-Chloro-1-indanone may be used as starting reagent for the preparation of 5-chloro-2-methoxycarbonyl-1-indanone. It may be used for the preparation of important biomedical compounds such as anticonvulsants, anticholinergics and diarylsulfonylureas, having potential activity against solid tumors.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Weak hydrogen-, halogen-and stacking Π....Π bonding in crystalline 5-chloro-1-indanone. An analysis by using X-ray diffraction, vibrational spectroscopy and theoretical methods.
Chemical Physics, 320(2), 164-180 (2006)
Synthesis of 5-Chloro-2-methoxycarbonyl-1-indanone [J].
Fine Chemicals / ????, 2, 022-022 (2009)
5, 6, 7-Trimethoxy-2, 3-dihydroinden-1-one.
Acta Crystallographica Section E, Structure Reports Online, 63(5), 2757-2757 (2007)
A facile synthesis of 7-halo-5H-indeno [1, 2-b] pyridines and-pyridin-5-ones.
The Journal of Organic Chemistry, 51(11), 2021-2023 (1986)
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