| Identification | More | [Name]
Novaluron | [CAS]
116714-46-6 | [Synonyms]
NOVALURON
RIMON
Benzamide, N-3-chloro-4-1,1,2-trifluoro-2-(trifluoromethoxy)ethoxyphenylaminocarbonyl-2,6-difluoro-
novaluron (bsi, pa e-iso)
N-[[3-Chloro-4-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]phenyl]carbamoyl]-2,6-difluorobenzamide | [Molecular Formula]
C17H9ClF8N2O4 | [MDL Number]
MFCD04112632 | [Molecular Weight]
492.7 | [MOL File]
116714-46-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
172-174° | [density ]
1.66 g/cm3 | [Fp ]
202℃ | [storage temp. ]
0-6°C | [solubility ]
DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly, Heated, Sonicated) | [form ]
neat | [pka]
8.68±0.46(Predicted) | [color ]
White to gray | [BRN ]
5465888 | [Major Application]
agriculture
environmental | [InChI]
1S/C17H9ClF8N2O4/c18-8-6-7(4-5-11(8)31-16(22,23)14(21)32-17(24,25)26)27-15(30)28-13(29)12-9(19)2-1-3-10(12)20/h1-6,14H,(H2,27,28,29,30) | [InChIKey]
NJPPVKZQTLUDBO-UHFFFAOYSA-N | [SMILES]
FC(OC(F)(F)F)C(F)(F)Oc1ccc(NC(=O)NC(=O)c2c(F)cccc2F)cc1Cl | [CAS DataBase Reference]
116714-46-6(CAS DataBase Reference) | [EPA Substance Registry System]
116714-46-6(EPA Substance) |
| Hazard Information | Back Directory | [Uses]
Insecticide. | [Uses]
Novaluron is an insect growth regulator and shows killing effect against various larvae of genus Lepidoptera, Coleoptera, Hemiptera and Diptera. | [Definition]
ChEBI: Novaluron is a benzoylurea insecticide, a member of monochlorobenzenes, an aromatic ether and an organofluorine compound. | [Production Methods]
The industrial synthesis of novaluron begins with the preparation of a key intermediate: 3-chloro-4-[1,1,2-trifluoro-2-(trifluoromethoxy)ethoxy]aniline. This intermediate is synthesised via an etherification reaction between trifluoromethoxytrifluoroethylene and 2-chloro-4-aminophenol, forming the complex fluorinated aromatic structure. The resulting aniline derivative is then acylated with 2,6-difluorobenzoyl chloride to form the benzoylphenyl backbone. Finally, the compound undergoes urea formation through reaction with isocyanates or carbodiimides, yielding the active novaluron molecule. These reactions are typically carried out in organic solvents such as acetonitrile or dichloromethane under controlled temperature and pH conditions to ensure high yield and purity. | [Mechanism of action]
Stomach action and some contact activity. Inhibitor of chitin biosynthesis affecting CHS1 | [storage]
Store at -20°C | [Pesticide Type]
Insecticide; Insect Growth Regulator |
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