3386-35-4 Usage
Description
P-Toluenesulfonic acid N-octyl ester, an organic compound belonging to the toluene sulfonic acids group, is derived from p-toluenesulfonic acid, a strong acid used as a catalyst in organic synthesis, and N-octanol, an eight-carbon alcohol. This chemical is a clear, colorless to pale yellow liquid with a faint odor. It is recognized for its ability to solubilize various organic compounds and its compatibility with a wide range of materials, making it a versatile and valuable chemical in the field of organic chemistry.
Uses
Used in Organic Synthesis:
P-Toluenesulfonic acid N-octyl ester is used as a reagent in organic synthesis for its ability to catalyze reactions, facilitating the formation of desired products and improving the efficiency of the synthesis process.
Used in Solvent Applications:
As a solvent, P-Toluenesulfonic acid N-octyl ester is used for its capacity to dissolve a variety of organic compounds, making it suitable for use in various chemical processes and formulations.
Used in Dispersant Applications:
P-Toluenesulfonic acid N-octyl ester is used as a dispersant in different industries to improve the distribution and stability of mixtures, preventing the aggregation of particles and ensuring a uniform composition.
Used in Emulsifying Agent Applications:
In the role of an emulsifying agent, P-Toluenesulfonic acid N-octyl ester helps to stabilize emulsions by reducing the interfacial tension between immiscible liquids, allowing for the formation of stable mixtures in various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3386-35-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3386-35:
(6*3)+(5*3)+(4*8)+(3*6)+(2*3)+(1*5)=94
94 % 10 = 4
So 3386-35-4 is a valid CAS Registry Number.
3386-35-4Relevant articles and documents
Cation and leaving group effects in isosorbide alkylation under microwave in phase transfer catalysis
Chatti, Saber,Bortolussi, Michel,Loupy, André
, p. 4365 - 4370 (2001)
We have studied cation, salt, leaving group effects and influence of catalyst under phase transfer catalysis conditions using concomitant microwave irradiation during di-n-octylation of isosorbide. A small amount of solvent was necessary to control temper
Combinatorial discovery of thermoresponsive cycloammonium ionic liquids
Chu, Yen-Ho,Hwang, Chun-Chieh,Chen, Chien-Yuan,Tseng, Min-Jen
supporting information, p. 11855 - 11858 (2020/10/13)
This work demonstrated, for the first time, the combinatorial discovery and rational identification of small-molecule cycloammonium-based thermoresponsive ionic liquids that exhibit LCST phase transition and carry attractiveTcvalues in water.
Cobalt-Catalyzed Silylcarbonylation of Unactivated Secondary Alkyl Tosylates at Low Pressure
Roque Pena, Joan E.,Alexanian, Erik J.
supporting information, p. 4413 - 4415 (2017/09/11)
A catalytic preparation of silyl enol ethers from unactivated secondary alkyl tosylates is reported. An inexpensive cobalt catalyst is used under mild conditions with low pressures of carbon monoxide. Nucleophilic, anionic cobalt carbonyls facilitate the catalytic activation of a range of alkyl tosylates. The silylcarbonylation offers a practical approach to synthetically valuable silyl enol ethers from simple starting materials.
