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CAS Number


 

β-D-Glucopyranoside, 4-hydroxyphenyl (C12H16O7)

Compound Descriptions:

Structure Drawing
Formula:C12H16O7
Molecular Weight:272.251 g/mol
Name(s):β-D-Glucopyranoside, 4-hydroxyphenyl
Arbutin
Glucopyranoside, p-hydroxyphenyl, β-D-
β-Arbutin
4-Hydroxyphenyl β-D-glucopyranoside
Arbutine
Hydroquinone β-D-glucopyranoside
p-Hydroxyphenyl β-D-glucopyranoside
p-Hydroxyphenyl β-D-glucoside
Ursin
Uvasol
arbutyne
quinol β-D-glucoside
p-Arbutin
Ericolin
Hydrochinon-β-D-glucopyranosid
Arbutoside
Hydroquinone-glucose
4-Hydroxyphenyl-β-D-glucopyranoside
CAS-RN:497-76-7, 30373-96-7
EINECS:207-850-3 EINECS
Classification:no charge; oxygen heterocycle; carbocycle; aromatic; alicycle; 6RingOnly; 6ring; alcohol; chiral; 1fragment

European Regulations

1 matching entries in european regulations: ECHA-pre

Derivatives / Analogues

Derivativestructure less defined: C12H16O7 
Analogueother nobel gas: C12H16O7 

Landolt-Börnstein Citations:

Spectroscopic Methods

 Nuclear Magnetic Resonance (NMR) Data - 13C: Vol. III/35d4 2.2:119III/35D4

References

III/35D4
Short: III/35D4
Title: Nuclear Magnetic Resonance (NMR) Data: Chemical Shifts for Carbon-13, Part 4: Natural Products
Author: Dobhal, M.P.
Editor: Gupta, R.R.; Lechner, M.D.
Source: Landolt-Börnstein, New Series
Volume: III/35D4
Year: 2006
Keyword: aromatic compounds; carbon-13; chemical shift; coupling constant; molecular structure
ISBN: 978-3-540-29732-1
ISBN: 3-540-29732-4
Internet Resource: DOI:10.1007/b13179
RefComment: VIII, 417 p., 1925 illus., Hardcover
RefComment: Written for Scientists and engineers in the fields of physics, chemistry and physical chemistry who intend 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, oriented 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)
  © 2009   Landolt Börnstein,   Springer-Verlag Berlin Heidelberg