64326-13-2

Basic information

• Product Name: SODIUMNAPHTHIONATE
• Synonyms: 1-NAPHTHALENESULFINIC ACID SODIUM SALT;Naphthalene-1-sulfinic acid sodium salt
• CAS NO: 64326-13-2
• Molecular Formula: C₁₀H₇O₂S*Na
• Molecular Weight: 0
• Mol File: 64326-13-2.mol
• Article Data: 20

Chemical Properties

• Appearance: /
• CAS DataBase Reference: SODIUMNAPHTHIONATE(CAS DataBase Reference)
• NIST Chemistry Reference: SODIUMNAPHTHIONATE(64326-13-2)
• EPA Substance Registry System: SODIUMNAPHTHIONATE(64326-13-2)

Safety Data

• Hazardous Substances Data: 64326-13-2(Hazardous Substances Data)

Upstream product

• 90-14-2 1-Iodonaphthalene 
• 529-36-2 1-Naphthalenethiol 
• 90-11-9 1-Bromonaphthalene 
• 85-46-1 1-Naphthalenesulfonyl chloride 
• 70310-90-6 N,N'-bis(diphenyloxyphosphonyl)-8-quinolinesulfinamidine 
• 85292-23-5 methyl β-(1-naphthylthio)-propionate 

Downstream Products

• 158752-55-7 2-(naphthalen-2-ylsulfonyl)-1-phenylethan-1-one 
• 252985-50-5 1-(naphthalen-1-ylsulfonyl)piperidine 
• 18506-76-8 1-(benzylsulfonyl)naphthalene 
• 61209-69-6 N-phenylnaphthalene-1-sulfonamide 
• 86-55-5 1-naphthalenecarboxylic acid 

Relevant articles and documents

Visible-Light-Induced, Palladium-Catalyzed 1,4-Difunctionalization of 1,3-Dienes with Bromodifluoroacetamides

A highly modular 1,4-difunctionalization of 1,3-dienes with bromodifluoroacetamides and sulfinates/amines through a photoinduced palladium-catalyzed radical relay process is described herein. This developed protocol offers a facile and general route to ac

Visible-light-promotedE-selective synthesis of α-fluoro-β-arylalkenyl sulfidesviathe deoxygenation/isomerization process

Regioselective synthesis of α-fluoro-β-arylalkenyl sulfides has been established withgem-difluoroalkenes and sodium sulfinates in a transition-metal-free manner. A series of control experiments were executed to demonstrate thiol radicals and anions as the proposed intermediates. Notably, regioselectiveZ→Eisomerization was achieved under green light irradiation in the absence of a photoinitiator.

Copper catalysed oxidative α-sulfonylation of branched aldehydes using the acid enhanced reactivity of manganese(iv) oxide

The oxidative coupling of secondary aldehydes and sulfinate salts is achieved using copper catalysis to form α-sulfonyl aldehydes. The use of an acidic co-solvent is important to adjust the oxidation potential of MnO2 as an oxidant. A broad range of sulfonylated aldehydes is prepared, and their further functionalisation is demonstrated. A dual ionic/radical pathway mechanism is proposed.