143-10-2 Usage
Description
1-Decanethiol is an alkanethiol that forms a self-assembled monolayer (SAM) and is characterized by its liquid chemical properties. It can be coated as a protective coating on a variety of substrates, making it a versatile compound with applications in various industries.
Uses
Used in Electronics Industry:
1-Decanethiol is used as a charge injection enhancer for improving the performance of field-effect transistors (FETs). It is applied by creating a monolayer on gold source-drain electrode surfaces, which aids in the efficient transfer of charge between the device and the electrodes.
Used in Nanotechnology and Surface Science:
1-Decanethiol is used as a component in the study of self-assembled monolayers (SAMs). These monolayers are crucial in nanotechnology and surface science for their ability to create well-ordered structures on surfaces, which can be utilized in various applications such as sensors, catalysts, and molecular electronics.
Used in Surface Protection and Coating Industry:
1-Decanethiol is used as a protective coating on a variety of substrates due to its ability to form a self-assembled monolayer. This application is beneficial in industries where surface protection and resistance to environmental factors are essential, such as aerospace, automotive, and industrial manufacturing.
Reactivity Profile
1-Decanethiol is incompatible with oxidizing agents, strong acids and bases, alkali metals, and nitric acid. May react with water, steam or acids to produce toxic and flammable vapors. Reacts violently with strong oxidizing agents such as calcium hypochlorite(Ca(OCl)2) forming toxic fumes of SOx. Will react with hydrides to form flammable H2 gas. May react with halogenated hydrocarbons to yield hydrogen halides. Reacts exothermically with aldehydes. May mit highly toxic fumes of SO when heated to decomposition.
Check Digit Verification of cas no
The CAS Registry Mumber 143-10-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143-10:
(5*1)+(4*4)+(3*3)+(2*1)+(1*0)=32
32 % 10 = 2
So 143-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H22S/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3
143-10-2Relevant articles and documents
ACTIVATION OF NITROSO GROUP WITH THIOLS. A NEW TRANSFORMATION OF PRIMARY AMINES TO ORGANIC SULFIDES OR THIOLS
Ueno, Yoshio,Tanaka, Chie,Okawara, Makoto
, p. 2675 - 2678 (1984)
Aliphatic primary amines reacted with 2-mercaptobenzothiazole in the presence of t-butylnitrite at room temperature to give condensation products, 2-(alkylthio)benzothiazole.
Amphiphilic dendrimer, synthesis method thereof, and application of amphiphilic dendrimer as drug delivery system
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Paragraph 0096-0097; 0108-0110, (2021/08/07)
The invention relates to a microenvironment response type amphiphilic dendrimer, a synthesis method thereof, and application of the microenvironment response type amphiphilic dendrimer as a drug delivery system. The microenvironment response type amphiphilic dendrimer is a compound with a structure as shown in a formula (I), a formula (II) or a formula (III) or pharmaceutically acceptable salt of the compound. The compound disclosed by the invention can be used as the nano delivery system based on tumor microenvironment specific response, has good solubility in an aqueous solution, can be self-assembled with a drug in the aqueous solution to form a relatively stable nano compound, can effectively deliver the loaded drug to a tumor site; and can responsively disassembl the nano-drug delivery carrier under corresponding stimulation to achieve the purpose of accurate drug release, so that the drug can be released to the focus part to the greatest extent, and the compound is a novel nano-delivery carrier.
Two-step three-component process for one-pot synthesis of 8-alkylmercaptocaffeine derivatives
Rad, M. N. Soltani,Maghsoudi
, p. 70335 - 70342 (2016/08/06)
A highly efficient, odourless and two-step three-component process for one-pot synthesis of some 8-alkylmercaptocaffeine derivatives has been described. The catalyst-free three-component reaction of alkyl bromides, thiourea, and 8-bromocaffeine gave 8-alkylmercaptocaffeine products in excellent to quantitative yields. In addition, the impact of parameters on sample reaction is discussed.