ChemicalBook--->CAS DataBase List--->14548-38-0

14548-38-0

14548-38-0 Structure

14548-38-0 Structure
IdentificationMore
[Name]

6-CHLORO-1-INDANONE 96
[CAS]

14548-38-0
[Synonyms]

6-CHLORO-1-INDANONE 96
6-Chloro-2,3-dihydro-1H-inden-1-one
[EINECS(EC#)]

627-183-5
[Molecular Formula]

C9H7ClO
[MDL Number]

MFCD00956388
[Molecular Weight]

166.6
[MOL File]

14548-38-0.mol
Chemical PropertiesBack Directory
[Melting point ]

71-79 °C
[Boiling point ]

110 °C(Press: 0.01 Torr)
[density ]

1.312±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

solid
[Appearance]

White to off-white Solid
[InChIKey]

SMSGJDOJSQHQIW-UHFFFAOYSA-N
[CAS DataBase Reference]

14548-38-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
[WGK Germany ]

2
[HazardClass ]

IRRITANT
[HS Code ]

2914790090
Hazard InformationBack Directory
[Uses]

6-Chloro-1-indanone is a chlorinated indanone compound. It is a crucial compound that could be used as a pharmaceutical intermediate in pharmaceutical synthesis and scientific research.
[Synthesis]

3-(4-Chlorophenyl)propanoic acid

2019-34-3

6-Chloro-1-indanone

14548-38-0

General procedure for the synthesis of 6-chloro-2,3-dihydroinden-1-one from 3-(4-chlorophenyl)propionic acid: trifluoromethanesulfonic acid (3 equiv.) was slowly added to an anhydrous solution of 3-(4-chlorophenyl)propionic acid (0.5 mmol) in anhydrous dichloromethane (1.0 mL) in a 12 mL Q-tube ?pressure tube (supplied by QLabtech) at 0 °C. . The reaction mixture was then warmed to room temperature. A PTFE septum was placed on top of the reaction tube and sealed using the appropriate cap and pressure adapter. The sealed reaction tube was heated in an oil bath at 80°C. The progress of the reaction was monitored by thin layer chromatography (TLC) and gas chromatography-mass spectrometry (GC/MS) until the feedstock completely disappeared. After completion of the reaction, the mixture was poured into ice water and extracted three times with dichloromethane. The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Finally, the target compound 6-chloro-2,3-dihydroinden-1-one was purified from the crude product by fast column chromatography.

[References]

[1] Molecules, 2014, vol. 19, # 5, p. 5599 - 5610
[2] Patent: WO2017/150904, 2017, A1. Location in patent: Paragraph 402-404
[3] Synthetic Communications, 2007, vol. 37, # 13, p. 2171 - 2177
[4] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 8, p. 2554 - 2558
[5] Polish Journal of Chemistry, 1991, vol. 65, # 11, p. 2057 - 2060
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLORO-1-INDANONE 96(14548-38-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

14548-38-0(sigmaaldrich)
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