130755-46-3

Basic information

• Product Name: 4,4'-dithiobis(5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile)
• Synonyms: 4,4'-dithiobis(5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile);1H-Pyrazole-3-carbonitrile,4,4'-dithiobis[5-aMino-1-[2,6-dichloro-4-(trifluoroMethyl)phenyl]-
• CAS NO: 130755-46-3
• Molecular Formula: C₂₂H₈Cl₄F₆N₈S₂
• Molecular Weight: 704.28
• EINECS: 423-490-1
• Mol File: 130755-46-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: >300 °C
• Boiling Point: 733.1oC at 760 mmHg
• Appearance: /
• Density: 1.83g/cm3
• Vapor Pressure: 0-0Pa at 20-50℃
• PKA: -2.82±0.21(Predicted)
• CAS DataBase Reference: 4,4'-dithiobis(5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-dithiobis(5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile)(130755-46-3)
• EPA Substance Registry System: 4,4'-dithiobis(5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile)(130755-46-3)

Safety Data

• Hazard Codes: N
• Statements: 50/53
• Safety Statements: 60-61
• Hazardous Substances Data: 130755-46-3(Hazardous Substances Data)

Usage

General Description

4,4'-dithiobis(5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile) is a chemical compound with a complex structure. It contains two pyrazole rings linked by a dithiobis group, and it also features amino and carbonitrile functional groups. The compound also contains chlorine and trifluoromethyl substituents. It has potential applications in the field of pharmaceuticals and materials due to its unique structure and functional groups. Additionally, the compound's properties make it ideal for further research and development in various industrial and scientific fields.

Upstream product

• 120068-79-3 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole 

Downstream Products

• 1088706-81-3 (Z)-3-(5-amino-3-cyano-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazol-4-ylthio)-N-methyl-N-phenylacrylamide 
• 1158997-76-2 C₁₅H₇Cl₂F₃N₄S₂ 
• 1158997-67-1 C₁₇H₈Cl₂F₄N₄S 
• 1158997-62-6 C₁₈H₁₁Cl₂F₃N₄S 
• 1158997-61-5 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(p-tolylthio)-1H-pyrazole-3-carbonitrile 
• 1158997-75-1 C₁₈H₉Cl₂F₃N₄O₂S 
• 1158997-71-7 C₁₈H₈Cl₂F₆N₄S 
• 1158997-72-8 C₁₈H₈Cl₂F₆N₄S 
• 1158997-64-8 C₁₉H₁₃Cl₂F₃N₄S 
• 1127335-86-7 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(phenylthio)-1H-pyrazole-3-carbonitrile 
• 1222566-19-9 C₁₇H₁₃Cl₆F₃N₄OS 
• 1222566-20-2 C₁₅H₁₀Cl₅F₃N₄O₂S 
• 1222566-21-3 C₁₆H₁₂Cl₅F₃N₄O₂S 
• 1222566-22-4 C₁₇H₁₄Cl₅F₃N₄O₂S 

Relevant articles and documents

Synthesis method of pyrazole disulfide

The invention discloses a synthesis method of pyrazole disulfide, which is realized through the following steps: 1) dissolving a pyrazole ring, and dissolving a pyrazole ring raw material in butyl acetate; adding a pre-weighed reducing agent into the solu

Substrate-Controlled [5+1] Annulation of 5-Amino-1H-phenylpyrazoles with Alkenes: Divergent Synthesis of Multisubstituted 4,5-Dihydropyrazolo[1,5-a]quinazolines

A new and efficient [5+1] annulation reaction for the first synthesis of 5,5-disubstituted 4,5-dihydropyrazolo[1,5-a]quinazolines is described. This transition-metal-free tandem cyclization was performed with 5-amino-1H-phenylpyrazole and readily availabl

Design, synthesis and insecticidal activity of novel phenylpyrazoles containing a 2,2,2-trichloro-1-alkoxyethyl moiety

A series of novel phenylpyrazoles containing a 2,2,2-trichloro-1- alkoxyethyl moiety were designed and synthesized via the key intermediate 5-trichloroethylideneimino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl) -4-alkylsulfenylpyrazole (5). The addition reaction of the imine 5 was closely related with the nature of the alcohol. The target compounds were confirmed by 1H NMR and elemental analysis. The results of bioassays indicated that the target compounds possessed excellent activities against a broad spectrum of insects such as bean aphid (Aphis craccivora), mosquito (Culex pipiens pallens) and diamondback moth (Plutella xylostella). Especially, the foliar contact activity against bean aphid of compound 7h at 2.5 mg kg -1 was 89%, the larvacidal activity against mosquito of compound 6c at 2.5 μg kg-1 was 100%, the activity against diamondback moth of compound 7a at 5 mg kg-1 was 87%, and all of these activities were much higher than the contrast ethiprole. The results of insecticidal activities showed that the two pairs of enantiomers 7d-1 and 7d-2 gave activities without distinctive difference, and it was the similar situation for 7e-1 and 7e-2. Interestingly, the target compounds exhibited high selectivity between diamondback moth and oriental armyworm, both of which are of the order Lepidoptera. The 2,2,2-trichloro-1-alkoxyethyl moiety was essential for high insecticidal activities.