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Merck
CN

433071

5-Chloro-1-indanone

99%

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About This Item

Empirical Formula (Hill Notation):
C9H7ClO
CAS Number:
Molecular Weight:
166.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
powder
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Product Name

5-Chloro-1-indanone, 99%

InChI

1S/C9H7ClO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2

SMILES string

Clc1ccc2C(=O)CCc2c1

InChI key

MEDSHTHCZIOVPU-UHFFFAOYSA-N

assay

99%

form

powder

mp

94-98 °C (lit.)

functional group

chloro
ketone

Quality Level

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.

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.

pictograms

Exclamation mark

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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5, 6, 7-Trimethoxy-2, 3-dihydroinden-1-one.
Saeed A and Bolte M.
Acta Crystallographica Section E, Structure Reports Online, 63(5), 2757-2757 (2007)
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.
Ruiz TP, et al.
Chemical Physics, 320(2), 164-180 (2006)
Synthesis of 5-Chloro-2-methoxycarbonyl-1-indanone [J].
HU X-G, et al.
Fine Chemicals / ????, 2, 022-022 (2009)
A facile synthesis of 7-halo-5H-indeno [1, 2-b] pyridines and-pyridin-5-ones.
DuPriest MT, et al.
The Journal of Organic Chemistry, 51(11), 2021-2023 (1986)

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