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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.
signalword
Warning
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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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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