10596-71-1 Usage
Uses
Used in Lubricant Additive Industry:
1-Octyldecylbenzene is used as a lubricant additive to enhance the performance and longevity of lubricants in various mechanical applications. Its high thermal and oxidation stability contribute to the improved durability and efficiency of the lubricants.
Used in Heat Transfer Fluid Industry:
As a heat transfer fluid, 1-Octyldecylbenzene is utilized in systems that require efficient heat exchange due to its thermal stability and low volatility. This makes it suitable for applications in industries such as automotive, aerospace, and chemical processing.
Used in Synthetic Resins and Rubbers Production:
1-Octyldecylbenzene is used as a component in the production of synthetic resins and rubbers, contributing to the development of materials with specific properties for various applications, including coatings, adhesives, and elastomers.
Used in Drilling and Cutting Oils Industry:
As a base fluid for drilling and cutting oils, 1-Octyldecylbenzene provides the necessary lubrication and cooling properties required in machining processes. Its low volatility and thermal stability ensure consistent performance and reduced wear on cutting tools.
It is important to handle and use 1-Octyldecylbenzene with care due to its potential health hazards and environmental impact. Proper safety measures and disposal methods should be followed to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 10596-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10596-71:
(7*1)+(6*0)+(5*5)+(4*9)+(3*6)+(2*7)+(1*1)=101
101 % 10 = 1
So 10596-71-1 is a valid CAS Registry Number.
10596-71-1Relevant articles and documents
Titanocene-Catalyzed Regioselective Carbomagnesation of Alkenes and Dienes
Nii, Shinsuke,Terao, Jun,Kambe, Nobuaki
, p. 573 - 576 (2004)
A new method for regioselective carbomagnesation of alkenes and dienes has been developed by the use of a titanocene catalyst. This reaction proceeds efficiently at 0 °C in THF in the presence of Cp2TiCl 2 by the combined use of organic halides (R-X; R = alkyl, aryl and vinyl) and n-BuMgCl to afford benzyl, α-silylalkyl, or allyl Grignard reagents, which were trapped with various electrophiles. The present reaction involves (i) addition of carbon radicals toward alkenes or dienes in the carbon-carbon bond-forming step and (ii) transmetalation on Ti of benzyl-α-silylalkyl-, or allyltitanocene with n-BuMgCl in the carbon-magnesium bond-forming step. The scope and limitations of this reaction have also been examined.
