96892-95-4 Usage
Description
2,6-Naphthalenedithiol is an organic compound with the chemical formula C10H8S2. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and features two thiol (-SH) groups attached to the 2nd and 6th carbon atoms. 2,6-Naphthalenedithiol is known for its unique chemical properties and potential applications in various industries.
Uses
Used in Polymer Industry:
2,6-Naphthalenedithiol is used as a monomer in the preparation of polyaromatic ether. Its presence in the polymer structure contributes to enhanced thermal stability and mechanical properties, making it suitable for high-performance materials in demanding applications.
Used in Chemical Industry:
In the chemical industry, 2,6-Naphthalenedithiol is used to manufacture silicone rubber. Its incorporation into the silicone rubber formulation improves the material's flexibility, durability, and resistance to environmental factors, making it ideal for a wide range of applications, including automotive, aerospace, and electronics.
Used in Cosmetic Industry:
2,6-Naphthalenedithiol is used as an active ingredient in a cosmetic process for attenuating wrinkles. Its ability to interact with proteins and other biomolecules in the skin may contribute to improved skin elasticity and a reduction in the appearance of fine lines and wrinkles, offering potential benefits in anti-aging skincare products.
Check Digit Verification of cas no
The CAS Registry Mumber 96892-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,9 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96892-95:
(7*9)+(6*6)+(5*8)+(4*9)+(3*2)+(2*9)+(1*5)=204
204 % 10 = 4
So 96892-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H8S2/c11-9-3-1-7-5-10(12)4-2-8(7)6-9/h1-6,11-12H
96892-95-4Relevant articles and documents
Dependence of single-molecule conductance on molecule junction symmetry
Taniguchi, Masateru,Tsutsui, Makusu,Mogi, Ryoji,Sugawara, Tadashi,Tsuji, Yuta,Yoshizawa, Kazunari,Kawai, Tomoji
, p. 11426 - 11429 (2011/10/04)
The symmetry of a molecule junction has been shown to play a significant role in determining the conductance of the molecule, but the details of how conductance changes with symmetry have heretofore been unknown. Herein, we investigate a naphthalenedithiol single-molecule system in which sulfur atoms from the molecule are anchored to two facing gold electrodes. In the studied system, the highest single-molecule conductance, for a molecule junction of 1,4-symmetry, is 110 times larger than the lowest single-molecule conductance, for a molecule junction of 2,7-symmetry. We demonstrate clearly that the measured dependence of molecule junction symmetry for single-molecule junctions agrees with theoretical predictions.
Process for preparation of aromatic thiols
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, (2008/06/13)
Disclosed is a process for preparation of an aromatic thiol corresponding to the structure wherein A is a substituted or unsubstituted aromatic radical and n is 1, 2, 3, 4, 5 or 6 comprising contacting at a temperature of at least 80° C. an aromatic halide corresponding to the structure wherein A is the same as above, X is bromine or iodine and n is 1, 2, 3, 4, 5, or 6 with thiourea in the presence of nickel metal.