Cas no 243971-02-0 (2-[4-(trifluoromethyl)phenyl]-1H-Indole)
243971-02-0 structure
Product Name:2-[4-(trifluoromethyl)phenyl]-1H-Indole
CAS No:243971-02-0
MF:C15H10F3N
MW:261.241814136505
CID:1109665
PubChem ID:10377944
Update Time:2025-04-20
2-[4-(trifluoromethyl)phenyl]-1H-Indole Chemical and Physical Properties
Names and Identifiers
-
- 2-[4-(trifluoromethyl)phenyl]-1H-Indole
- 1H-Indole, 2-[4-(trifluoromethyl)phenyl]-
- 2-(4-(trifluoromethyl)phenyl)1H-indole
- 2-(4-(trifluoromethyl)phenyl)-1H-indole
- 2-(4-[trifluoromethyl]phenyl)-1H-indole
- 2-(4-trifluoromethylphenyl)-1H-indole
- 2-(4-trifluoromethyl-phenyl)-1H-indole
- 2-[(4-trifluoromethyl)-phenyl]-1H-indole
- CTK0J4949
- SureCN4893046
- DTXSID00438985
- HS-7821
- 2-[4-Trifluoromethyl)phenyl]-1H-indole
- 1H-Indole,2-[4-trifluoromethyl)phenyl]-
- SCHEMBL4893046
- 243971-02-0
-
- MDL: MFCD05224906
- Inchi: 1S/C15H10F3N/c16-15(17,18)12-7-5-10(6-8-12)14-9-11-3-1-2-4-13(11)19-14/h1-9,19H
- InChI Key: QZPAJNQQHGFLSK-UHFFFAOYSA-N
- SMILES: FC(C1C=CC(=CC=1)C1=CC2C=CC=CC=2N1)(F)F
Computed Properties
- Exact Mass: 261.0766
- Monoisotopic Mass: 261.07653381g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 19
- Rotatable Bond Count: 2
- Complexity: 307
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 4.7
- Topological Polar Surface Area: 15.8?2
Experimental Properties
- PSA: 15.79
2-[4-(trifluoromethyl)phenyl]-1H-Indole Related Literature
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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3. Estimating and correcting interference fringes in infrared spectra in infrared hyperspectral imagingGhazal Azarfar,Ebrahim Aboualizadeh,Nicholas M. Walter,Simona Ratti,Camilla Olivieri,Alessandra Norici,Michael Nasse,Achim Kohler,Mario Giordano Analyst, 2018,143, 4674-4683
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Xingqun Zheng,Lele Song,Xin Feng,Li Li,Zidong Wei J. Mater. Chem. A, 2020,8, 14145-14151
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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