3839-35-8 Usage
Description
P-TOLUENESULFONIC ACID N-HEXYL ESTER, also known as Hexyl p-Toluenesulfonate, is an organic compound that serves as a versatile reactant in various chemical synthesis processes. It is characterized by its ability to facilitate the formation of complex organic molecules, making it a valuable component in the production of pharmaceuticals and other specialty chemicals.
Uses
Used in Pharmaceutical Synthesis:
P-TOLUENESULFONIC ACID N-HEXYL ESTER is used as a reactant in the synthesis of 7-bromo-5-(2''-chlorophenyl)-3-hydroxy-1-methyl-1,2-dihydro-3H-1,4-benzodiazepin-2-one 1 and 7-bromo-5-(2''-chloro)phenyl-1-hexyl-1,2,4,5-tetrahydro-3H-1,4-benzodiazepin-2,3-dione. These compounds are important in the development of pharmaceuticals, particularly those targeting central nervous system disorders and other therapeutic applications.
Used in Carbazate Synthesis:
In the chemical industry, P-TOLUENESULFONIC ACID N-HEXYL ESTER is also utilized in the synthesis of carbazates. Carbazates are a class of compounds that have potential applications in various fields, including as intermediates for the production of pharmaceuticals, agrochemicals, and other specialty chemicals. The use of Hexyl p-Toluenesulfonate in this process highlights its versatility and importance in the synthesis of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 3839-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3839-35:
(6*3)+(5*8)+(4*3)+(3*9)+(2*3)+(1*5)=108
108 % 10 = 8
So 3839-35-8 is a valid CAS Registry Number.
3839-35-8Relevant articles and documents
Synthesis of polyfluorinated ethers
Bazhin,Gorbunova,Zapevalov,Saloutin
, p. 1646 - 1650 (2005)
Procedures for preparing polyfluorinated ethers H(CF2CF 2)nCH2OR by alkylation of the corresponding telomeric alcohols H(CF2CF2)nCH2OH (n = 1-3) with alkyl halides and alkyl tosylates were examined.
Combinatorial discovery of thermoresponsive cycloammonium ionic liquids
Chu, Yen-Ho,Hwang, Chun-Chieh,Chen, Chien-Yuan,Tseng, Min-Jen
, 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.
Hexyl triazabutadiene as a potent alkylating agent
Knyazeva, Diana C.,Kimani, Flora W.,Blanche, Jean-Laurent,Jewett, John C.
, p. 2700 - 2702 (2017/06/23)
Alkyl diazonium ions are among the most reactive alkylating agents in the synthetic chemists’ arsenal. That said, there are precious few methods by which one can selectively and safely utilize this chemistry. Herein, we show the use of a bench stable hexyl triazabutadiene as a source of reactive diazonium ions that undergo substitution chemistry with weak nucleophiles, such as carboxylates and even sulfonates. In the absence of a nucleophile, elimination was observed to occur. To overcome issues stemming from side-product inhibition of the reaction, we show that the triazabutadiene can be pre-activated with tosyl isocyanate.
