1127335-86-7

Basic information

• Product Name: 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(phenylthio)-1H-pyrazole-3-carbonitrile
• Synonyms: 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(phenylthio)-1H-pyrazole-3-carbonitrile
• CAS NO: 1127335-86-7
• Molecular Weight: 429.252
• Mol File: 1127335-86-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(phenylthio)-1H-pyrazole-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(phenylthio)-1H-pyrazole-3-carbonitrile(1127335-86-7)
• EPA Substance Registry System: 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(phenylthio)-1H-pyrazole-3-carbonitrile(1127335-86-7)

Safety Data

• Hazardous Substances Data: 1127335-86-7(Hazardous Substances Data)

Upstream product

• 130755-46-3 4,4'-dithiobis [5-amino-3-cyano-1-{2,6-dichloro-4-(trifluoromethyl)phenyl}-1H-pyrazole] 
• 98-80-6 phenylboronic acid 
• 882-33-7 diphenyldisulfane 
• 120068-79-3 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole 
• 2996-92-1 phenyl trimethylsiloxane 

Relevant articles and documents

Solvent-free copper-catalyzed oxidative S-arylation of 1,2-diaryldisulfides with aryltrimethoxysilane

A novel and solvent-free protocol for the synthesis of diarylsulfides by the copper-catalyzed oxidative S-arylation of 1,2-diaryldisulfides with aryltrimethoxysilanes is reported. In the presence of CuI, 2-(di-tert-butylphosphino)biphenyl, and TBAF (n-Bu

Iron-catalyzed direct sulfenylation and selenylations of phenylpyrazoles: Synthesis of fipronil derivatives with disulfides promoted by a catalytic amount of iodine

The direct thiolation of phenylpyrazole with disulfide using the FeBr 3/I2 complex as the catalyst in MeCN at 80 °C was reported. With the optimum conditions, several fipronil derivatives of 4-sulfenylpyrazole were synthesized by the reaction of 5-amino-1-[2,6-dichloro- 4-(trifluoromethyl)phenyl-lH-pyrazole-3-arbonitrile (1a) with disulfides (2) in moderate to good yields. The coupling reaction with diaryl diselane also occurred under similar conditions.