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线性分子式:
C10H7SH
化学文摘社编号:
分子量:
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
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
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
Rakesh K Pandey et al.
Journal of colloid and interface science, 315(2), 528-536 (2007-08-19)
We have formed the cholesterol monolayer and multilayer LB films on the self-assembled monolayers of 2-naphthalenethiol (2-NT) and thiophenol (TP) and studied the electrochemical barrier properties of these composite films using cyclic voltammetry and electrochemical impedance spectroscopy. We have also
Peng Jiang et al.
Journal of the American Chemical Society, 128(38), 12390-12391 (2006-09-21)
We evidence by STM that 2-naphthalenethiol self-assembled monolayers formed at the n-tetradecane/Au(111) interface coexist as two structural phases which both possess molecules into two different orientations (standing and lying). Such a rotational polymorphism is observed and understood at the molecular
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