W331401
2-Naphthalenethiol
99%
Synonym(s):
2-Naphthyl mercaptan, Thio-2-naphthol (β)
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About This Item
Linear Formula:
C10H7SH
CAS Number:
Molecular Weight:
160.24
Flavis number:
12.033
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3314
EC Number:
202-082-5
MDL number:
Beilstein/REAXYS Number:
636389
SMILES string
Sc1ccc2ccccc2c1
InChI
1S/C10H8S/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
InChI key
RFCQDOVPMUSZMN-UHFFFAOYSA-N
biological source
synthetic
assay
99%
bp
286 °C (lit.)
application(s)
flavors and fragrances
organoleptic
sulfurous
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Surface-enhanced Raman scattering for ultrasensitive chemical analysis of 1 and 2-naphthalenethiols.
R A Alvarez-Puebla et al.
The Analyst, 129(12), 1251-1256 (2004-11-27)
The results of the search for the optimal experimental conditions for ultrasentitive chemical analysis of 1-naphthalenethiol (1-NAT) and 2-naphthalenethiol (2-NAT) using surface-enhanced Raman scattering (SERS) are discussed. The report begins with a review of the vibrational spectra, including infrared and
J Ni et al.
Analytical chemistry, 71(21), 4903-4908 (1999-11-24)
An immunoassay readout method based on surface-enhanced Raman scattering (SERS) is described. The method exploits the SERS-derived signal from reporter molecules that are coimmobilized with biospecific species on gold colloids. This concept is demonstrated in a dualanalyte sandwich assay, in
Metal-cluster catalysts: Access granted.
Graham J Hutchings
Nature chemistry, 2(12), 1005-1006 (2010-11-26)
A bioinspired approach for controlling accessibility in calix[4]arene-bound metal cluster catalysts.
Namal de Silva et al.
Nature chemistry, 2(12), 1062-1068 (2010-11-26)
In enzymes, the electronic and steric environments of active centres, and therefore their activity in biological processes, are controlled by the surrounding amino acids. In a similar manner, organic ligands have been used for the 'passivation' of metal clusters, that
Richard A van Delden et al.
Organic & biomolecular chemistry, 2(10), 1531-1541 (2004-05-12)
Insight in the steric and electronic parameters governing isomerization processes in artificial molecular motors is essential in order to design more advanced motor systems. A subtle balance of steric parameters and the combination of helical and central chirality are key
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