1370337-81-7

Basic information

• Product Name: 3-bromo-1-(3-chloropyridin-2-yl)-N-(2,4-dichloro-6-cyanophenyl)-1H-pyrazole-5-carboxamide
• Synonyms: 3-bromo-1-(3-chloropyridin-2-yl)-N-(2,4-dichloro-6-cyanophenyl)-1H-pyrazole-5-carboxamide
• CAS NO: 1370337-81-7
• Molecular Weight: 471.527
• Mol File: 1370337-81-7.mol

Chemical Properties

• CAS DataBase Reference: 3-bromo-1-(3-chloropyridin-2-yl)-N-(2,4-dichloro-6-cyanophenyl)-1H-pyrazole-5-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-1-(3-chloropyridin-2-yl)-N-(2,4-dichloro-6-cyanophenyl)-1H-pyrazole-5-carboxamide(1370337-81-7)
• EPA Substance Registry System: 3-bromo-1-(3-chloropyridin-2-yl)-N-(2,4-dichloro-6-cyanophenyl)-1H-pyrazole-5-carboxamide(1370337-81-7)

Safety Data

• Hazardous Substances Data: 1370337-81-7(Hazardous Substances Data)

Upstream product

• 500011-86-9 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid 
• 943982-60-3 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carbonyl chloride 
• 36764-94-0 2-amino-3,5-dichlorobenzonitrile 
• 1006623-99-9 C₁₆H₉BrCl₃N₅O₂ 

Relevant articles and documents

Synthesis and structure-insecticidal activity relationship of novel phenylpyrazole carboxylic acid derivatives containing fluorine moiety

A series of novel phenylpyrazole carboxylic acid derivatives containing fluorine moiety, i.e., diamides 11, simple aryl-bearing amides 12 and acylthioureas 14 were successfully synthesized based on the key fluoro-containing phenylpyrazole acid intermediate. The new compounds were identified and confirmed by melting point, 1H NMR, 13C NMR and elemental analysis or HRMS. The bioassay results indicated that some of the compounds possessed excellent insecticidal activities towards oriental armyworm, diamondback moth and corn borer at low concentrations. For examples, compounds 11a, 11e?g and 14b exhibited remarkable larvicidal activities with LC50 values of 0.13 ? 0.39 mg/L and 0.0002 ? 0.0014 mg/L against oriental armyworm and diamondback moth, respectively, were comparable with those of the control chlorantraniliprole. Particularly, 11e were found superior to chlorantraniliprole in oriental armyworm tests (LC50: 0.23 mg/L vs. 0.26 mg/L); 11a, 11e, 11f and 14c in diamondback moth tests with LC50 values of 0.0002 mg/L, 0.0002 mg/L, 0.0008 mg/L and 0.0005 mg/L, respectively, were more effective than that of chlorantraniliprole. In addition, 12a also showed a promising insecticidal potential and development/optimization advantage. Compounds 11a, 11e–g, 12a, 14b and 14c could be considered as possible new leading structures for further study. The SAR investigation indicated that the compounds with fluorine motif (e.g., -F, -CF2H, -CF3) held apparently favorable insecticidal potentials, which provided useful guidance for further design/development of new phenylpyrazole-containing agrochemicals.

O-AMINO BENZONITRILE COMPOUNDS, METHOD FOR PREPARING SAME AND USES THEREOF

It relates to an anthranilonitrile compound, and to the process for preparing the said anthranilonitrile compound, and to its use. The anthranilonitrile compound has a chemical general formula (I). The compound of the general formula (I) has excellent pesticidal activity, can be used to control pests, and has more than 98% of mortality in 3 days to diamondback moth and pink borer.