1254961-52-8

Basic information

• Product Name: Cl(CH₂)10O(C₆H₂-2,4,6-Me₃)
• CAS NO: 1254961-52-8
• Molecular Weight: 310.908
• Mol File: 1254961-52-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Cl(CH₂)10O(C₆H₂-2,4,6-Me₃)(CAS DataBase Reference)
• NIST Chemistry Reference: Cl(CH₂)10O(C₆H₂-2,4,6-Me₃)(1254961-52-8)
• EPA Substance Registry System: Cl(CH₂)10O(C₆H₂-2,4,6-Me₃)(1254961-52-8)

Safety Data

• Hazardous Substances Data: 1254961-52-8(Hazardous Substances Data)

Upstream product

• 2162-98-3 1,10-dichlorodecane 
• 527-60-6 Mesitol 

Downstream Products

• 1254961-47-1 [4,4'-bpy-N-(CH₂)10O(C₆H₂-2,4,6-Me₃)](+)*Cl^(1-) 

Relevant articles and documents

Reversible formation and destruction of micelles of amphiphilic compounds in aqueous media. competition with pseudorotaxane formation

N-Alkyl-4,4′-bipyridiniums [4,4′-bpy-N-(CH2) nOAr]+(Cl-) (n = 6 and 10, Ar = C 6H3-3,5-t-Bu2, C6H 3-3,5-(OMe)2, and C6H2-2,4,6-Me 3), having the cationic bipyridinium group and a long hydrophobic alkyl chain, were prepared from the reaction of 4,4′-bipyridine with the corresponding alkyl chlorides. The amphiphilic compounds in water form micelles which encapsulate added pyrene in the hydrophobic core. Addition of α-cyclodextrin to the micellar solution converts a part of the aggregated amphiphilic molecules to their pseudorotaxane with α-cyclodextrin. Formation of the pseudorotaxanes is favored at lower temperature, as is observed by temperature dependent change of the absorption spectra.