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Chemical Name


1-naphthaleneethanoic acid (C12H10O2)

Compound Descriptions:

Structure Drawing
Formula:C12H10O2
Molecular Weight:186.207 g/mol
Name(s):1-naphthaleneethanoic acid
ethanoic acid, 1-naphthalene-
1-naphthaleneacetic acid
α-NAA
α-Naphthaleneacetic acid
α-Naphthylacetic acid
1-NAA
1-Naphthylacetic acid
2-(α-Naphthyl)ethanoic acid
2-(1-Naphthyl)acetic acid
Agronaa
Alman
ANU
Biokor
Celmone
Etifix
Fruitofix
Fruitone N
N 10
Nafusaku
Phyomone
Planofix
Planofixe
Pomoxon
Rasin
Rhizopon B
Rhodofix
Tre-hold
Vardhak
(1)naphthyl-acetic acid
α-Naphthylessigsäure
naphthalen-1-yl-acetic acid
Naphthalene acetic acid
1-naphthylethanoic acid
α-Naphthyleneacetic acid
Alphaspra
Appl-Set
ANA
Klingtite
Liqui-Stik
Naphthalene-1-acetic acid
Naphyl-1-essigsäure
Niagara-Stik
Nu-Tone
Parmone
Phymone
Pimacol-Sol
Primacol
Rootone
Stafast
Stop-Drop
Tekkam
Tip-Off
Transplantone
1-Naphthtaleneacetic acid
1-Naphthylessigsäure
Naphthalin-1-essigsäure
α-Naphthylacethydrazide
1-Naphthalinessigsäure
CAS-RN:86-87-3, 61913-11-9
EINECS:201-705-8 EINECS
Classification:no charge; carbocycle; aromatic; large ring; fused rings; 6ring; 10ring; carboxylic acid; 1fragment

European Regulations

1 matching entries in european regulations: ECHA-pre

Landolt-Börnstein Citations:

Spectroscopic Methods

Thermodynamic Properties

 Thermodynamic Properties of Organic Compounds and Their Mixtures: Vol. IV/8a 3.5.6, p.282IV/8A

References

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.
IV/8A
Short: IV/8A
Title: Enthalpies of Fusion and Transition of Organic Compounds
Author: Zhang, Z.-Y.; Frenkel, M.; March, K.N.; Wilhoit, R.C.
Editor: Marsh, K.N.
Source: Landolt-Börnstein, New Series
Volume: IV/8A
Year: 1995
Keyword: organic compounds; enthaly of fusion; melting point; phase transition
ISBN: 3-540-58854-X
ISBN: 978-3-540-58854-2
Internet Resource: DOI:10.1007/b55145
RefComment: VIII, 588 pages.
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)
  © 2009   Landolt Börnstein,   Springer-Verlag Berlin Heidelberg