7133-26-8 Usage
Uses
Used in Pharmaceutical Industry:
(Hexylthio)cyclohexane is used as an intermediate in the synthesis of various pharmaceutical products. Its chemical structure allows it to be a versatile building block for the development of new drugs and medications.
Used in Pesticide Industry:
In the pesticide industry, (Hexylthio)cyclohexane is employed as a component in the formulation of different types of pesticides. Its properties make it suitable for use in creating effective and targeted pest control solutions.
Used in Perfume Industry:
(Hexylthio)cyclohexane is used as a component in fragrance formulations. Its distinct odor and stability contribute to the creation of various scents and perfumes, enhancing the sensory experience of consumers.
Used as a Solvent in Organic Synthesis:
(Hexylthio)cyclohexane serves as a solvent in organic synthesis, facilitating chemical reactions and improving the efficiency of the synthesis process. Its compatibility with a range of organic compounds makes it a valuable asset in the field of chemistry.
Safety Precautions:
It is crucial to handle (Hexylthio)cyclohexane with care, as it may pose health risks if ingested, inhaled, or comes into contact with the skin. Adhering to proper safety protocols and guidelines is essential to minimize potential hazards when working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 7133-26-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7133-26:
(6*7)+(5*1)+(4*3)+(3*3)+(2*2)+(1*6)=78
78 % 10 = 8
So 7133-26-8 is a valid CAS Registry Number.
7133-26-8Relevant academic research and scientific papers
The Regioselective Reaction of Atomic Hydrogen with Unsymmetric Disulfides and Sulfides
Tanner, Dennis D.,Zhang, Liying,Vigneswaran, Markandu,Kandanarachchi, Pramod
, p. 4481 - 4487 (2007/10/02)
Unsymmetrical disulfides undergo solution phase reduction with atomic hydrogen regioselectively by displacement at the least hindered sulfur atom.The cleavage of the sulfur-sulfur bond forms mixtures of two thiol and two thiyl radicals.At the temperature at which the reactions are carried out, the thiyl radicals form symmetric disulfides by thiyl-thiyl radical coupling and not by thiyl radical displacement on the starting material.The reaction of atomic hydrogen with an unsymmetric sulfide is a cleavage that favors the formation of the most stable radical.The reaction of phenyl cyclohexyl sulfide produces benzene, cyclohexane, cyclohexyl thiol, and thiophenol.Benzene and cyclohexyl thiol produced from the cleavage of the phenyl-sulfur bond are proposed to arise from the α-scission of an intermediate formed by ipso-addition of atomic hydrogen to the benzene ring.
