6873-86-5

Basic information

• Product Name: Benzenesulfinamide, 4-methyl-N-(1-methylethyl)-
• CAS NO: 6873-86-5
• Molecular Formula: C10H15NOS
• Molecular Weight: 197.301
• Mol File: 6873-86-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfinamide, 4-methyl-N-(1-methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfinamide, 4-methyl-N-(1-methylethyl)-(6873-86-5)
• EPA Substance Registry System: Benzenesulfinamide, 4-methyl-N-(1-methylethyl)-(6873-86-5)

Safety Data

• Hazardous Substances Data: 6873-86-5(Hazardous Substances Data)

Upstream product

• 67-64-1 acetone 
• 188447-91-8 (S)-p-toluenesulfinimide 
• 672-78-6 (-)-(S)-methyl toluene-p-sulphinate 
• 75-31-0 isopropylamine 
• 10439-23-3 4-methylbenzenesulfinyl chloride 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 1858-86-2 Ethyl p-toluenesulfinate 

Downstream Products

• 1059194-07-8 C₂₂H₂₇BNOPS 
• 27094-01-5 N-isopropyl-N-diphenylphosphinyl-p-toluolsulfinamid 
• 105-36-2 ethyl bromoacetate 
• 145835-13-8 ethyl 2-(p-tolylsulfinyl)acetate 
• 111289-39-5 [Isopropyl-((S)-toluene-4-sulfinyl)-amino]-acetic acid tert-butyl ester 
• 672-78-6 methyl p-toluene sulfinate 
• 116560-15-7 4-Methyl-benzenesulfinic acid isopropyl-methyl-amide 
• 116560-16-8 [Isopropyl-(toluene-4-sulfinyl)-amino]-acetic acid tert-butyl ester 
• 36160-75-5 C₁₃H₁₉NO₃S 
• 36160-74-4 2-[Isopropyl-(toluene-4-sulfinyl)-amino]-N-propyl-acetamide 
• 21230-07-9 N-isopropyl-p-toluenesulfonamide 

Relevant articles and documents

N-phosphino-p-tolylsulfinamide ligands: Synthesis, stability, and application to the intermolecular Pauson-Khand reaction

(Chemical Equation Presented) Here we synthesized a family of racemic and optically pure N-phosphino-p-tolylsulfinamide (PNSO) ligands. Their stability and coordination behavior toward dicobalt-alkyne complexes was evaluated. Selectivities of up to 3:1 we

Syntheses and Reactions of Optically Active Alkyltoluene-p-sulphinamides. Part 2. Substitution at Sulphur with Retention of Configuration

The stereochemistry of the reaction of optically active sulphonamides (1a-c) with different alkylating agents has been examined.The electrophilic attack on sulphoximidate anions occurs only at nitrogen.Prevailing retention of configuration at sulphur (e.e. up to 48percent) is observed in the formation of p-tolylsulphinyl acetates from sulphinamides (1b-c) with α-bromo esters.