41563-69-3 Usage
Description
1,3-Benzenedimethanethiol is an organic compound with the chemical formula C8H10S2. It is characterized by its adsorption properties on gold (Au) surfaces, which have been studied using various techniques such as surface-enhanced Raman scattering, UV/Vis absorption spectroscopy, and cyclic voltammetry (CV).
Uses
Used in Surface Science and Nanotechnology:
1,3-Benzenedimethanethiol is used as an adsorbate for gold surfaces in surface science and nanotechnology applications. Its interaction with the Au surface is crucial for understanding the fundamental properties of metal-organic interfaces and can be utilized in the development of novel sensors, catalysts, and electronic devices.
Used in Analytical Chemistry:
In analytical chemistry, 1,3-benzenedimethanethiol is employed as a probe molecule for studying the surface properties of gold nanoparticles and thin films. Its adsorption behavior provides insights into the surface chemistry and reactivity of gold surfaces, which can be applied to improve the sensitivity and selectivity of analytical methods.
Used in Material Science:
1,3-Benzenedimethanethiol can be used as a component in the synthesis of new materials with tailored properties. Its interaction with gold surfaces can be exploited to create self-assembled monolayers or multilayers, which can be applied in various fields such as corrosion protection, lubrication, and molecular electronics.
Used in Pharmaceutical Research:
Although not explicitly mentioned in the provided materials, 1,3-benzenedimethanethiol may have potential applications in the pharmaceutical industry due to its sulfur-containing structure. It could be used as a building block for the synthesis of new drugs or as a modifier to improve the solubility, stability, or bioavailability of existing pharmaceutical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 41563-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,6 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41563-69:
(7*4)+(6*1)+(5*5)+(4*6)+(3*3)+(2*6)+(1*9)=113
113 % 10 = 3
So 41563-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10S2/c9-5-7-2-1-3-8(4-7)6-10/h1-4,9-10H,5-6H2
41563-69-3Relevant articles and documents
POLYTHIOL COMPOSITION AND METHOD FOR PRODUCING SAME
-
Paragraph 0034-0035, (2017/09/13)
The present invention provides a polythiol composition containing, as the main component, a polythiol compound (a) having two or more mercapto groups, and containing 0.5% by mass or less of a nitrogen-containing compound (b) in which at least one mercapto group in the polythiol compound (a) is substituted with a group represented by formula (1).
A convenient method for regeneration of free thiol from a tert-butyl thioether
Kragulj, Elijah J.,Gustafson, Jeffery L.,Grotjahn, Douglas B.
, p. 2851 - 2854 (2008/02/13)
When dimethylmethylthiosulfonium triflate (DMTST) is added to a tert-butyl-protected thiol (RSt-Bu), the unsymmetrical disulfide RSSMe is formed. At this point the free thiol (RSH) can be obtained by the addition of trimethylphosphine and water. Most byproducts are small organic molecules that are easily removed. Georg Thieme Verlag Stuttgart.
THE SYNTHESIS AND CHARACTERIZATION OF SOME NEW THIOETHER-IMIDAZOLE CONTAINING LIGANDS.
Bouwman, E.,Driessen, W. L.
, p. 1581 - 1588 (2007/10/02)
Procedures are described involving a convenient condensation of 4(5)-hydroxymethylimidazole or 5-methyl-4-hydroxymethylimidazole with several thiols.The main step, the condensation reaction in refluxing acetic acid, is essentially the same for all ligands
