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Chemical Name


 

N-(4-Fluoro-phenyl)-acetamide (C8H8FNO)

Compound Descriptions:

Structure Drawing
Formula:C8H8FNO
Molecular Weight:153.154 g/mol
Name(s):N-(4-Fluoro-phenyl)-acetamide
N-(4-fluorophenyl)acetamide
Acetamide, N-(4-fluorophenyl)-
acetic acid-(4-fluoro-anilide)
p-Fluoroacetanilide
Acetanilide, 4'-fluoro-
4-Fluoroacetanilide
4'-Fluoroacetanilide
4'-Fluoracetanilid
N1-(4-fluorophenyl)acetamide
N-(4-Fluorphenyl)-acetamid
CAS-RN:351-83-7
EINECS:206-515-9 EINECS
Classification:no charge; carbocycle; aromatic; 6RingOnly; 6ring; amide; 1fragment

European Regulations

1 matching entries in european regulations: ECHA-pre

Derivatives / Analogues

Analogueother halogene: N-(4-Bromo-phenyl)-acetamide 
Analogueother halogene: 4-chlorophenylethanamide 
Analogueother halogene: Acetamide, N-(4-iodophenyl-)- 

Landolt-Börnstein Citations:

Spectroscopic Methods

 Nuclear Magnetic Resonance (NMR) Data - 13C: Vol. III/35d2 2.4, p.52III/35D2
 Nuclear Magnetic Resonance (NMR) Data - 19F & 15N: Vol. III/35b 3.2:867, p.176III/35B

References

III/35B
Short: III/35B
Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts and Coupling Constants for Fluorine-19 and Nitrogen-15
Author: Balasubramanian, M.; Gupta, R.R.; Jain, M.; Perumal, S.
Editor: Gupta, R.R.; Lechner, M.D.
Source: Landolt-Börnstein, New Series
Volume: III/35B
Year: 1998
ISBN: 3-540-63275-1
ISBN: 978-3-540-63275-7
Internet Resource: DOI:10.1007/b55685
RefComment: VII, 242 pages. With CD-ROM. Hardcover
Abstract: This volume provides a comprehensive and evaluated compilation of nuclear magnetic resonance data. Chemical shifts and coupling constants of boron-11 and phosphorus-31 (subvol. A), fluorine-19 and nitrogen-15 (subvol. B), hydrogen-1 (subvol. C), and carbon-13 (subvol. D) compounds are tabulated together with the gross- and structure formulas and the most readily available solvents. Due to the large amount of the data merely chemical shifts are presented in the printed versions, and all the data, chemical shifts and coupling constants are provided on CO-ROM's.
III/35D2
Short: III/35D2
Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Carbon-13, Part 2: Aromatic Compounds
Author: Mikhova, B.
Editor: Gupta, R.R.; Lechner, M.D.
Source: Landolt-Börnstein, New Series
Volume: III/35D2
Year: 2005
Keyword: aromatic compounds; carbon-13; chemical shift; coupling constant; molecular structure
ISBN: 978-3-540-20189-2
ISBN: 3-540-20189-0
Internet Resource: DOI:10.1007/b83345
RefComment: VIII, 291 p., Hardcover
RefComment: Written for Science and engineers in the fields of physics, chemistry and physical chemistry who inted to use NMR to study the structure and the binding of molecules
Abstract: Nuclear Magnetic Resonance (NMR) is based on the fact that certain nuclei exhibit a magnetic moment, orient by a magnetic field, and absorb characteristic frequencies in the radiofrequency part of the spectrum. The spectral lines of the nuclei are highly influenced by the chemical environment i.e. the structure and interaction of the molecules. NMR is now the leading technique and a powerful tool for the investigation of the structure and interaction of molecules. The present Landolt-Börnstein volume III/35 Nuclear Magnetic Resonance (NMR) Data is therefore of major interest to all scientists and engineers who intend to use NMR to study the structure and the binding of molecules. Volume III/35 "NMR-Data" is divided into several subvolumes and parts. Subvolume III/35A contains the nuclei 11B and 31P, subvolume III/35B contains the nuclei 19F and 15N, subvolume III/35C contains the nucleus 1H, subvolume III/35D contains the nucleus 13C, subvolume III/35E contains the nucleus 17O, and subvolume III/35G contains the nucleus 77Se. More nuclei will be presented later.
EINECS
Short: EINECS
Title: EINECS (European Inventory of Existing Commercial Chemical Substances)
Source: Official Journal of the European Communities
Volume: C 146 A (15.06.1990)
Page: 1
Year: 1990
Publish_Date: 1990/06/15

  File created on 2009/18/08 by LCI Publisher GmbH (Gaja Peters, Inga Thede, Volkmar Vill, Ron Zenczykowski)
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