1309569-14-9

Basic information

• Product Name: 1-Nitro-2-benzenesulfoxylmethyl-4-(pentafluorosulfanyl)benzene
• Synonyms: 1-Nitro-2-benzenesulfoxylmethyl-4-(pentafluorosulfanyl)benzene
• CAS NO: 1309569-14-9
• Molecular Weight: 403.351
• Mol File: 1309569-14-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Nitro-2-benzenesulfoxylmethyl-4-(pentafluorosulfanyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Nitro-2-benzenesulfoxylmethyl-4-(pentafluorosulfanyl)benzene(1309569-14-9)
• EPA Substance Registry System: 1-Nitro-2-benzenesulfoxylmethyl-4-(pentafluorosulfanyl)benzene(1309569-14-9)

Safety Data

• Hazardous Substances Data: 1309569-14-9(Hazardous Substances Data)

Usage

Nitro-containing organic compound

The presence of the -NO2 group makes it a nitro compound, which can undergo various chemical reactions and has specific properties.

Benzene and sulfoxyl functional groups

The compound contains both benzene rings and sulfoxyl (-SO) groups, which contribute to its chemical reactivity and stability.

Pentafluorosulfanyl group

A unique feature of the compound is the presence of a pentafluorosulfanyl (-S(O)5F) group, consisting of a sulfur atom covalently bonded to five fluorine atoms.

Unique chemical and physical properties

The pentafluorosulfanyl group imparts special properties to the compound, making it useful in various applications.

Potential use as a source of highly electrophilic sulfur(VI) fluoride anion

The compound can be used as a source of this valuable reagent in organic synthesis, which can further react with other compounds to form new products.

Applications in the pharmaceutical industry

Due to its unique molecular structure and properties, the compound may find use in the development of new drugs and therapeutic agents.

Applications in material science

The compound's unique properties may also make it suitable for use in the development of new materials and technologies.

Upstream product

• 2613-27-6 1-nitro-4-(pentafluorosulfanyl)benzene 
• 7205-98-3 chloromethyl phenyl sulfone 

Downstream Products

• 1394319-46-0 2-(4-bromophenyl)-5-(pentafluorosulfanyl)-1H-indole 
• 1394319-69-7 2-phenyl-5-(pentafluorosulfanyl)-1H-indole 
• 1446255-10-2 2-(4-methoxyphenyl)-5-(pentafluorosulfanyl)-1H-indole 
• 1394319-64-2 2-(4-chlorophenyl)-5-(pentafluorosulfanyl)-1H-indole 
• 1446250-18-5 [2-benzenesulfonylmethyl-4-(pentafluorosulfanyl)phenyl]-(4-bromobenzylidine)-amine 
• 1446250-16-3 [2-benzenesulfonylmethyl-4-(pentafluorosulfanyl)phenyl]-benzylidineamine 
• 1446250-14-1 [2-benzenesulfonylmethyl-4-(pentafluorosulfanyl)phenyl]-(4-methoxybenzylidine)-amine 
• 1446250-11-8 [2-benzenesulfonylmethyl-4-(pentafluorosulfanyl)phenyl]-(4-chlorobenzylidine)-amine 
• 1446250-10-7 4-(pentafluoro-λ⁶-sulfanyl)-2-((phenylsulfonyl)methyl)aniline 

Relevant articles and documents

Synthesis of pentafluorosulfanyl-containing indoles and oxindoles

Vicarious nucleophilic substitution (VNS) of 3- and 4- nitro(pentafluorosulfanyl)benzenes with phenoxyacetonitrile followed by catalytic hydrogenation provided a two-step, atom-economical synthetic route to 6- and 5-(pentafluoro-sulfanyl)-1H-indoles. The

Synthesis of 5-pentafluorosulfanyl indazoles

An efficient method for the synthesis of 5-SF5 substituted indazoles from commercially available 4-nitro-(pentafluorosulfanyl)benzene through vicarious nucleophilic substitution of hydrogen (VNS) reaction, reduction of nitro group and cyclizati

Preparation of SF5 aromatics by vicarious nucleophilic substitution reactions of nitro(pentafluorosulfanyl)benzenes with carbanions

Vicarious nucleophilic substitutions (VNS) of hydrogen in 1-nitro-4-(pentafluorosulfanyl)benzene with carbanions provide 2-substituted 1-nitro-4-(pentafluorosulfanyl)benzenes in good to high yields. VNS of 1-nitro-3-(pentafluorosulfanyl)benzene gives a mi