51148-67-5

Basic information

• Product Name: 10-Undecen-1-ol, 4-methylbenzenesulfonate
• Synonyms: 10-undecene-1-tosylate;10-Undecen-1-ol,4-methylbenzenesulfonate;toluene-4-sulfonic acid undec-10-enyl ester;10-undecen-1-ol p-toluenesulfonate;undec-10-enyl 4-methylbenzenesulfonate;10-undecen-1-yl p-toluenesulfonate;undec-10-enyl 4-methylbenzenesulphonate
• CAS NO: 51148-67-5
• Molecular Formula: C18H28O3S
• Molecular Weight: 324.485
• Mol File: 51148-67-5.mol
• Article Data: 28

Chemical Properties

• CAS DataBase Reference: 10-Undecen-1-ol, 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 10-Undecen-1-ol, 4-methylbenzenesulfonate(51148-67-5)
• EPA Substance Registry System: 10-Undecen-1-ol, 4-methylbenzenesulfonate(51148-67-5)

Safety Data

• Hazardous Substances Data: 51148-67-5(Hazardous Substances Data)

Upstream product

• 112-43-6 10-Undecen-1-ol 
• 4124-41-8 p-toluenesulfonylanhydride 
• 112-38-9 10-undecenoic acid 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 110458-66-7 4-(undec-10-en-1-yloxy)benzaldehyde 
• 5048-44-2 11-dodecenenittrile 
• 7766-50-9 1-undecen-11-ylbromide 
• 83932-93-8 10-eicosenyl-1,20-ditosylate 
• 83932-88-1 10-eicosenyl-1,20-ditosylate 
• 66605-82-1 11-hydroxyundecyl 4-methylbenzenesulfonate 
• 148773-56-2 11-(phenylthio)-1-undecene 
• 59100-95-7 4-(10-undecenyloxy)benzoic acid 
• 129401-84-9 C₁₇H₂₅IO 
• 1105562-24-0 1-(trimethylsilyl)-2-(4-(10-undecenyloxy)phenyl)acetylene 
• 1344155-25-4 triethoxy-(11-(4-((trimethylsilyl)ethynyl)phenoxy)undecyl)silane 
• 1446088-39-6 C₁₉H₃₂O₄S 
• 1446088-40-9 C₂₂H₃₈O₄S 
• 114996-87-1 11-(phenylseleno)-1-undecene 

Relevant articles and documents

PREPARATION ET PROPRIETES SOLUBILISANTES DE MICELLES POLYMERISEES D'UN TENSIOACTIF GLYCOLIPIDIQUE: LE POLY (N-(UNDECENE-10-YL)LACTOBIONAMIDE)

We have investigated the micellar properties of an amphiphilic carbohydrate-containing molecule, the N-(undecen-10-yl)lactobionamide (1) as well as those of its corresponding polymer 2 obtained by γ-irradiation.Comparative studies showed a better efficien

Synthesis of precision ionic polyolefins derived from ionic liquids

The synthesis of ionic polyolefins derived from ionic liquid (IL) monomers with the use of acyclic diene metathesis polymerization was anzlyzed. The metathesis polycondensation of a fully ionic monomer was accomplished by preparing ionic monomers that are

A mesoporous silica functionalized by a covalently bound calixarene-based fluoroionophore for selective optical sensing of mercury(II) in water

With the aim of optical sensing of Hg2+ in water, a calixarene bearing two dansyl fluorophores was grafted on a large pore mesoporous silica material (SBA-15) via two long alkyl chains containing triethoxysilane groups. The characterization of

Visible Light-Gated Cobalt Catalysis for a Spatially and Temporally Resolved [2+2+2] Cycloaddition

The ability to exert spatial and temporal control over a transition-metal catalyst offers diverse opportunities for the fabrication of functional materials. Using an external stimulus such as visible light to toggle a catalyst between an active and dorman

Total synthesis and antifungal activity of (2S,3R)-2-aminododecan-3-ol

We report the total synthesis of (2S,3R)-2-aminododecan-3-ol has been achieved starting from commercially available 10-undecenoic acid. The key steps involved are Sharpless asymmetric epoxidation, Miyashita's boron-directed C-2 regioselective azidolysis, generated the asymmetric centers and in situ detosylation and reduction of azido tosylate. The antifungal activity of the synthesized (2S,3R)-2-aminododecan-3-ol was evaluated on several Candida strains and was comparable to miconazole, a standard drug.