60835-11-2 Usage
Uses
Used in Lubricant Additives:
(Octadecylsulfanyl)benzene is used as an additive in the lubricant industry to enhance the performance and efficiency of lubricants. Its long-chain structure contributes to better lubrication and reduces friction between moving parts.
Used in Chemical Production:
(Octadecylsulfanyl)benzene serves as an intermediate in the production of various chemicals, highlighting its importance in the chemical industry.
Used in Polymer and Plastic Manufacturing:
(octadecylsulfanyl)benzene is utilized in the manufacturing process of polymers and plastics, where it contributes to the desired properties of the final products, such as flexibility and durability.
Used in Surfactant Production:
(Octadecylsulfanyl)benzene is also employed in the production of surfactants, which are essential in various industries, including cosmetics, pharmaceuticals, and cleaning products, for their emulsifying and stabilizing properties.
Used in Specialty Chemicals:
It is a component in the formulation of specialty chemicals, where its unique properties are harnessed for specific applications.
Used in Agricultural Chemicals:
(Octadecylsulfanyl)benzene is also used in the production of agricultural chemicals, where it may contribute to the effectiveness of pesticides or fertilizers.
Check Digit Verification of cas no
The CAS Registry Mumber 60835-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,3 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60835-11:
(7*6)+(6*0)+(5*8)+(4*3)+(3*5)+(2*1)+(1*1)=112
112 % 10 = 2
So 60835-11-2 is a valid CAS Registry Number.
60835-11-2Relevant articles and documents
Deoxygenation of sulfoxides and selenoxides with nickel boride
Khurana, Jitender M.,Ray, Abhijit,Singh, Sarika
, p. 3829 - 3832 (2007/10/03)
The deoxygenations of a variety of acyclic sulfoxides and selenoxides have been reported with nickel boride in THF at 0-5°C in nearly quantitative yields. The deoxygenations are proposed to proceed by an oxidative-addition and reductive-elimination mechanism.
Hydrozirconation of oleyl sulphides and oleyl phenylsulphone
Karlsson, Susanne,Hallberg, Anders,Gronowitz, Salo
, p. 53 - 60 (2007/10/02)
The hydrozirconation of 9-(Z)-octadecenylmethyl-sulphide, 9-(Z)-octadecenyl phenyl sulphide and 9-(Z)-octadecenyl phenyl sulphone have been studied.These compounds underwent substantial elimination of the functional group, yielding after hydrolysis, along with saturated and unsaturated sulphides and sulphones, large amount of octadecane.The saturated analogues (dodecylmethyl-sulphide, octadecyl phenyl sulphide and octadecylphenyl sulphone) were unaffected by the hydrozirconation reagent under similar conditions.
