82031-33-2 Usage
Uses
Used in Plastics and Polymers Industry:
2-(2-Methoxyethoxy)benzenesulfonamide is used as a plasticizer for enhancing the flexibility and workability of plastics and polymers, such as polyurethane. It helps improve the flow and processing properties of these materials, making them easier to mold and shape.
Used in Lubricants:
2-(2-Methoxyethoxy)benzenesulfonamide is used as a lubricant in various applications, reducing friction between surfaces and improving the efficiency of mechanical systems.
Used as an Antistatic Agent:
2-(2-Methoxyethoxy)benzenesulfonamide is used as an antistatic agent to prevent the buildup of static electricity in materials, which can be crucial in industries where electrostatic discharge could cause damage or safety hazards.
Used in Corrosion Inhibition:
2-(2-Methoxyethoxy)benzenesulfonamide serves as a corrosion inhibitor, protecting metal surfaces from corrosion and extending the lifespan of equipment and structures.
Used in Pharmaceutical and Crop Protection Products:
2-(2-Methoxyethoxy)benzenesulfonamide is used as a component in the formulation of pharmaceuticals and crop protection products, contributing to their effectiveness and performance.
It is important to handle and use 2-(2-Methoxyethoxy)benzenesulfonamide with proper safety precautions, as it can cause irritation to the eyes, skin, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 82031-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,3 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82031-33:
(7*8)+(6*2)+(5*0)+(4*3)+(3*1)+(2*3)+(1*3)=92
92 % 10 = 2
So 82031-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO4S/c1-13-6-7-14-8-4-2-3-5-9(8)15(10,11)12/h2-5H,6-7H2,1H3,(H2,10,11,12)
82031-33-2Relevant academic research and scientific papers
Process for producing sulfonylureas
-
, (2008/06/13)
There is described a novel process for producing sulfonylureas of formula I STR1 wherein R1 is hydrogen or alkyl, R2 is STR2 E is =N-- or =CH--, R3 is alkyl, alkoxy or halogen, R4 is alkyl, cycloalkyl, alkoxy, halogen, alkoxy-alkyl, halo-alkyl or halo-alkoxy, R5 is hydrogen or alkyl, T is a substituted phenyl group STR3 Y is hydrogen or halogen, X is hydrogen, halogen, alkyl, halo-alkyl, alkenyl, halo-alkenyl, alkynyl, alkoxy, halo-alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, halo-alkylthio, alkylsulfonyloxy, phenylsulfonyloxy, phenylsulfonyloxy mono- or polysubstituted by alkyl, or is di-alkylsulfamoyl, and A is a bridge member which has 3 or 4 atoms and which contains 1 or 2 hetero atoms, selected from the group consisting of oxygen, sulfur and nitrogen, the said process comprising reacting a silfonamide of the formula II in the presence of a base, with diphenyl carbonate to form a salt of a phenyl carbamate converting this salt into the free phenyl carbamate and reacting this further with an amine. Sulfonylureas are herbicidally effective compounds.
N-Phenylsulfonyl-N'-triazinylureas
-
, (2008/06/13)
N-Phenylsulfonyl-N'-triazinylureas of the general formula STR1 and the salts thereof with amines, alkali metal or alkaline earth metal bases or with quaternary ammonium bases, have good pre- and postemergence selective herbicidal and growth regulating pro
N-Phenylsulfonyl-N'-pyrimidinylureas
-
, (2008/06/13)
N-Phenylsulfonyl-N'-pyrimidinylureas of the general formula STR1 and the salts thereof with amines, alkali metal or alkaline earth metal bases or with quaternary ammonium bases, have good pre- and postemergence selective herbicidal and growth regulating p
