ChemicalBook--->CAS DataBase List--->16618-72-7

16618-72-7

16618-72-7 Structure

16618-72-7 Structure
IdentificationBack Directory
[Name]

3-PHENYL-1-INDANONE
[CAS]

16618-72-7
[Synonyms]

Nsc 82364
Brn 1370263
AKOS BC-0964
3-Phenylindanone
3-phenyl-1-indanon
TIMTEC-BB SBB008151
3-PHENYLINDAN-1-ONE
3-PHENYL-1-INDANONE
1-Indanone, 3-phenyl-
3-phenyl-2,3-dihydroinden-1-one
2,3-dihydro-3-phenyl-1h-inden-1-on
3-phenyl-2,3-dihydro-1H-inden-1-one
2,3-Dihydro-3-phenyl-1H-inden-1-one
3-Phenyl-2,3-dihydro-1H-indene-1-one
(3S)-3-phenyl-2,3-dihydroinden-1-one
1H-Inden-1-one, 2,3-dihydro-3-phenyl-
1H-Indene-1-one, 2,3-dihydro-3-phenyl-
1H-Inden-1-one, 2,3-dihydro-3-phenyl- (9ci)
[Molecular Formula]

C15H12O
[MDL Number]

MFCD00037722
[MOL File]

16618-72-7.mol
[Molecular Weight]

208.26
Chemical PropertiesBack Directory
[Melting point ]

75-78 °C(lit.)
[Boiling point ]

148 °C0.7 mm Hg(lit.)
[density ]

1.162
[refractive index ]

1.5361 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[InChI]

1S/C15H12O/c16-15-10-14(11-6-2-1-3-7-11)12-8-4-5-9-13(12)15/h1-9,14H,10H2
[InChIKey]

SIUOTMYWHGODQX-UHFFFAOYSA-N
[SMILES]

O=C1CC(c2ccccc2)c3ccccc13
[CAS DataBase Reference]

16618-72-7
Questions And AnswerBack Directory
[Uses]

3-Phenyl-1-indanone can be used as a pharmaceutical synthesis intermediate and can be used in laboratory research and development processes.
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[Safety Statements ]

36
[WGK Germany ]

3
[RTECS ]

NK7538200
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
[Toxicity]

mouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02960,
Spectrum DetailBack Directory
[Spectrum Detail]

3-PHENYL-1-INDANONE(16618-72-7)IR
3-PHENYL-1-INDANONE(16618-72-7)FT-IR
Hazard InformationBack Directory
[Synthesis]

Under the protection of high-purity nitrogen, 0.05 mmol of heteronuclear ruthenium-palladium bicyclic metal compound 1, 1 mmol of o-iodoacetophenone, 2.5 mmol of benzyl alcohol, 2 mmol of potassium hydroxide, and 3 ml of dioxin were added to a 10 ml Schle
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