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185663

Sigma-Aldrich

5-Fluoro-1-indanone

99%

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About This Item

Empirical Formula (Hill Notation):
C9H7FO
CAS Number:
700-84-5
Molecular Weight:
150.15
MDL number:
MFCD00041031
UNSPSC Code:
12352100
PubChem Substance ID:
24851156
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

99%

form

solid

bp

113-114 °C (lit.)

mp

38-40 °C (lit.)

density

1.216 g/mL at 25 °C (lit.)

functional group

fluoro
ketone

SMILES string

Fc1ccc2C(=O)CCc2c1

InChI

1S/C9H7FO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2

InChI key

WVPPBVAMKNQXJA-UHFFFAOYSA-N

Application

5-Fluoro-1-indanone was used to prepare precursor for thiosemicarbazones derived from 1-indanones[1]. It was used in the synthesis of 6-fluoro-1,2,3,4-tetrahydroquinoline hydrochloride[2].

Pictograms

Exclamation mark
GHS07

Signal Word

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ2802
MKCJ7182
MKBB1435
99297PJ
05210PE

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Satoshi Sakami et al.
Bioorganic & medicinal chemistry, 16(17), 7956-7967 (2008-08-15)
We have previously reported on antitussive effect of (5R,9R,13S,14S)-17-cyclopropylmethyl-6,7-didehydro-4,5-epoxy-5',6'-dihydro-3-methoxy-4'H-pyrrolo[3,2,1-ij]quinolino[2',1':6,7]morphinan-14-ol(1b) methanesulfonate (TRK-850), a selective delta opioid receptor antagonist which markedly reduced the number of coughs in a rat cough model. We designed TRK-850 based on naltrindole (NTI), a typical delta opioid
María E Caputto et al.
Bioorganic & medicinal chemistry, 19(22), 6818-6826 (2011-10-18)
In the present work, we synthesized a series of thiosemicarbazones derived from 1-indanones with good anti-Trypanosoma cruzi activity. Most of them displayed remarkable trypanosomicidal activity. All the compounds showed nonspecific cytotoxicity on human erythrocytes. The ability of the new compounds

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