1077-56-1 Usage
Uses
Used in Plasticizer Applications:
N-Ethyl-o-toluenesulfonamide is used as a plasticizer to enhance the flexibility and workability of materials in products such as adhesives, coatings, and polymers. Its ability to improve the physical properties of these materials without significantly affecting their chemical structure makes it a valuable additive.
Used in Anti-corrosion Applications:
In the metalworking industry, N-Ethyl-o-toluenesulfonamide is utilized as an anti-corrosion agent in metalworking fluids. It helps to prevent the corrosion of metal surfaces during manufacturing processes, thereby extending the life of the machinery and the end products.
Used in High-Temperature Applications:
Due to its excellent thermal stability, N-Ethyl-o-toluenesulfonamide is suitable for use in high-temperature applications where other compounds may degrade or lose their effectiveness. This makes it an ideal choice for industries that require materials to perform reliably under extreme conditions.
Safety Precautions:
It is crucial to handle N-Ethyl-o-toluenesulfonamide with care, as it can be harmful if ingested or inhaled and can cause irritation to the skin and eyes. Therefore, proper safety precautions and handling procedures should be followed to ensure the well-being of individuals working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 1077-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1077-56:
(6*1)+(5*0)+(4*7)+(3*7)+(2*5)+(1*6)=71
71 % 10 = 1
So 1077-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO2S/c1-3-10-13(11,12)9-7-5-4-6-8(9)2/h4-7,10H,3H2,1-2H3
1077-56-1Relevant academic research and scientific papers
Dong, Xiang,Sang, Rui,Wang, Qiang,Tang, Xiang-Ying,Shi, Min
, p. 16910 - 16915 (2013)
A multi-talented system: An efficient copper-catalyzed tandem trifluoromethylation/annulation of an electron-deficient aromatic ring has been developed. This method provides a powerful and straightforward way to synthesize trifluoromethylated 1,2-benzothiazinane dioxides under mild conditions (see scheme). The mechanism was investigated by a series of kinetic experiments and isotopic labeling studies.
