112906-44-2

Basic information

• Product Name: Cyclohexanol, 4,4-dimethoxy-
• CAS NO: 112906-44-2
• Molecular Formula: C8H16O3
• Molecular Weight: 160.213
• Mol File: 112906-44-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexanol, 4,4-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 4,4-dimethoxy-(112906-44-2)
• EPA Substance Registry System: Cyclohexanol, 4,4-dimethoxy-(112906-44-2)

Safety Data

• Hazardous Substances Data: 112906-44-2(Hazardous Substances Data)

Upstream product

• 150-76-5 4-methoxy-phenol 
• 67-56-1 methanol 
• 13482-22-9 4-hydroxycyclohexanone 
• 220061-72-3 (4,4-dimethoxy-cyclohexyloxymethyl)-benzene 
• 69125-55-9 4-hydroxy-1-methoxy-1-cyclohexene 
• 149-73-5 trimethyl orthoformate 

Downstream Products

• 251324-90-0 C₁₁H₂₀O₃ 
• 124549-78-6 methoxymethyl ether of 1,1-dimethoxy-4-hydroxy-4-(2'-pyridyl)cyclohexane 
• 124568-67-8 1,1-dimethoxy-4-hydroxy-4-(2'-pyridyl)cyclohexane 
• 124549-79-7 methoxymethyl ether of 1,1-dimethoxy-4-hydroxy-4-(2'-piperidyl)cyclohexane 
• 124549-74-2 4-hydroxy-1-methoxy-4-(2'-piperidyl)cyclohex-1-ene 
• 124549-70-8 1,1-dimethoxy-4-hydroxy-4-(2'-piperidyl)cyclohexane 
• 56180-50-8 4,4-dimethoxycyclohexan-1-one 

Relevant articles and documents

Synthesis and properties of isomerically pure anthrabisbenzothiophenes

The synthesis of three heptacyclic heteroacenes is described, namely anthra[2,3-b:7,6-b′]bis[1]benzothiophenes (ABBTs). A stepwise sequence of aldol reactions provides regiochemical control, affording only the syn-isomer. The ABBTs are characterized by X-ray crystallography, UV-vis absorption, and emission spectroscopy, as well as cyclic voltammetry. Field effect transistors based on solution-cast thin films of ABBT derivatives exhibit charge-carrier mobilities of as high as 0.013 cm2/(V s).

Selective acceleration for deprotection of benzyl ethers with ti-HMS

Ti-HMS, a Ti-loaded hexagonal mesoporous silica, was found to accelerate deprotection of benzyl ethers under hydrogenolytic conditions with palladium catalyst. Such acid-sensitive functional groups as silyl ether and acetal moieties in the molecule were little affected by Ti-HMS, which possesses Lewis acid sites due to Ti-atom.