66605-77-4

Basic information

• Product Name: 9-Decen-1-ol, 4-methylbenzenesulfonate
• CAS NO: 66605-77-4
• Molecular Formula: C17H26O3S
• Molecular Weight: 310.458
• Mol File: 66605-77-4.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 9-Decen-1-ol, 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Decen-1-ol, 4-methylbenzenesulfonate(66605-77-4)
• EPA Substance Registry System: 9-Decen-1-ol, 4-methylbenzenesulfonate(66605-77-4)

Safety Data

• Hazardous Substances Data: 66605-77-4(Hazardous Substances Data)

Upstream product

• 13019-22-2 9-Decen-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 100566-35-6 2-Phenyl-3-(9-decenyloxy)-7-ethoxycarbonylmethylthio-pyrazolo[4,3-d]pyrimidine 
• 1429183-64-1 2-(9-decenyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione 
• 1429183-59-4 2-(10-Cyclohexyldecyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione 
• 53179-04-7 undec-10-enenitrile 
• 117560-76-6 methyl 4-(dec-9-enyloxy)benzoate 
• 5129-57-7 methyl 11-methyldodecanoate 
• 1437766-21-6 N-(tert-butoxycarbonyl)bis[4-[(dec-9-en-1-yloxy)methyl]benzyl]amine 
• 1430812-83-1 C₂₀H₃₀O₂ 

Relevant articles and documents

Novel phenolic antioxidant-functionalized dendritic polyethylene: Synthesis by tailor-made nickel(II) α-diimine-catalyzed copolymerization and its characteristics as non-releasing additive

This work describes a simple one-pot and controlled synthetic method to generate migration-resistant bio-friendly tailor-made antioxidants through ethylene–sterically hindered phenolic antioxidant (SHPA) copolymerization by coordination polymerization usi

Photooxidation Kinetics in Heterogeneous Media

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Metal-Free Activation of C-I Bonds and Perfluoroalkylation of Alkenes with Visible Light Using Phosphine Catalysts

An efficient metal-free, photomediated iodo perfluoroalkylation under mild conditions was developed. Using catalytic amounts (10 mol %) of phosphines and blue light irradiation, various olefins are transformed into the corresponding addition products with

Branch-Selective Addition of Unactivated Olefins into Imines and Aldehydes

Radical hydrofunctionalization occurs with ease using metal-hydride hydrogen atom transfer (MHAT) catalysis to couple alkenes and competent radicalophilic electrophiles. Traditional two-electron electrophiles have remained unreactive. Herein we report the reductive coupling of electronically unbiased olefins with imines and aldehydes. Iron catalysis allows addition of alkyl-substituted olefins into imines through the intermediacy of free radicals, whereas a combination of catalytic Co(Salt-Bu,t-Bu) and chromium salts enables a branch-selective coupling of olefins and aldehydes through the formation of a putative alkyl chromium intermediate.