935447-39-5

Basic information

• Product Name: sodium 3-fluorobenzenesulfinate
• Synonyms: sodium 3-fluorobenzenesulfinate
• CAS NO: 935447-39-5
• Molecular Weight: 182.151
• Mol File: 935447-39-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: sodium 3-fluorobenzenesulfinate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium 3-fluorobenzenesulfinate(935447-39-5)
• EPA Substance Registry System: sodium 3-fluorobenzenesulfinate(935447-39-5)

Safety Data

• Hazardous Substances Data: 935447-39-5(Hazardous Substances Data)

Upstream product

• 701-27-9 3-fluorobenzene-1-sulfonyl chloride 

Downstream Products

• 1253422-82-0 C₂₂H₂₅FN₄O₄S 
• 1253422-86-4 C₂₂H₂₅FN₄O₄S 
• 936618-92-7 2-(3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 2106-20-9 3-((trifluoromethyl)sulfonyl)fluorobenzene 
• 1020734-56-8 1-(benzylsulfonyl)-3-fluorobenzene 
• 62942-25-0 (3-fluorophenyl)tri-n-butyltin 

Relevant articles and documents

Enhancing the Potential of Miniature-Scale DNA-Compatible Radical Reactions via an Electron Donor-Acceptor Complex and a Reversible Adsorption to Solid Support Strategy

DNA-encoded library (DEL) technology is a powerful tool in the discovery of bioactive probe molecules and drug leads. Mostly, the success in DEL technology stems from the molecular diversity of the chemical libraries. However, the construction of DELs has been restricted by the idiosyncratic needs and the required low concentration (～1 mM or less) of the library intermediate. Here, we report visible-light-promoted on-DNA radical coupling reactions via an electron donor-acceptor (EDA) complex and a reversible adsorption to solid support (RASS) strategy. This protocol provides a unique solution to the challenges of increasing the reactivity of highly diluted DNA substrates and reducing the residues of heavy metals from photocatalysts. A series of on-DNA indole sulfone and selenide derivatives were obtained with good to quantitative conversions. It is anticipated that these mild-condition on-DNA radical reactions will significantly improve the chemical diversity of DELs and find widespread utility to DEL construction.

2-AMINO-N-(ARYLSULFINYL)-ACETAMIDE COMPOUNDS AS INHIBITORS OF BACTERIAL AMINOACYL-TRNA SYNTHETASE

The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain 2-amino-N-(arylsulfinyl)- acetamide compounds that, inter alia, inhibit (e.g., selectively inhibit) bacterial amino

Copper-mediated oxysulfonylation of alkenyl oximes with sodium sulfinates: a facile synthesis of isoxazolines featuring a sulfone substituent

A novel and efficient Cu(OAc)2-mediated oxysulfonylation of alkenyl oximes with sodium sulfonates was developed. The reactions are easy to conduct, occur under mild conditions, and form a broad range of sulfone-substituted isoxazolines in good yields.