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1 2-dihydro-2 2 4-trimethylquinoline cas no 147-47-7 rubber antioxidant rd
1 2-dihydro-2 2 4-trimethylquinoline cas no 147-47-7 rubber antioxidant rd
1 2-dihydro-2 2 4-trimethylquinoline cas no 147-47-7 rubber antioxidant rd
1 2-dihydro-2 2 4-trimethylquinoline cas no 147-47-7 rubber antioxidant rd
1 2-dihydro-2 2 4-trimethylquinoline cas no 147-47-7 rubber antioxidant rd
  • Is 1 2 dihydro 2 2 4 trimethylquinoline combustible?
  • 1,2-Dihydro-2,2,4-trimethylquinoline is combustible. Moderately toxic by ingestion. When heated to decomposition it emits toxic fumes of NOx. The CAS Registry Mumber 147-47-7 includes 6 digits separated into 3 groups by hyphens.
  • What is 1 2 dihydro 2 2 4 trimethyl quinoline?
  • * Refer to Certificate of Analysis for lot specific data. 1,2-dihydro-2,2,4-trimethylquinoline (2,2,4-Trimethyl-1,2-dihydroquinoline) is a significant heterocyclic aromatic compound utilized as a intermediate in the synthesis of various pharmaceuticals and compounds.
  • What is 1 2 dihydroxy 2 2 4 trimethylquinoline used for?
  • 1,2-DIHYDRO-2,2,4-TRIMETHYLQUINOLINE (147-47-7) neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
  • Is 1,2 dihydro 2 2 4 trimethylquinoline mutagenic in Salmonella typhimurium?
  • GENETIC TOXICOLOGY: 1,2-Dihydro-2,2,4-trimethylquinoline was not mutagenic in any of several strains of Salmonella typhimurium, with or without S9 metabolic activation. 1,2-Dihydro-2,2,4-trimethylquinoline induced sister chromatid exchanges in cultured Chinese hamster ovary cells in the absence of S9, but not in the presence of S9.
  • What is the synthesis process of 2 2 4 trimethyl-1 2 dihydroquinolines?
  • A mild, convenient, and efficient process has been developed for the synthesis of 2,2,4-trimethyl-1,2-dihydroquinolines by the reaction of anilines with acetone catalyzed by ytterbium (III) triflate [Yb (OTf)3] in ionic liquids.
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