112906-44-2

Upstream product

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

Downstream Products

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

Relevant academic research and scientific papers

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).

SUBSTITUTED SPIROCYCLIC KETOENOLS

The invention relates to novel substituted spirocyclic ketoenols of formula (I), wherein W, X, Y, Z, A, B, D, and G have the meaning indicated above, several methods for the production thereof, and the use thereof as pesticides, microbiocides, and herbici

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.

SYNTHESIS OF 1-HYDROXY-7-AZATRICYCLO2.7>DODECAN-9-ONES: POTENTIAL INTERMEDIATES FOR THE TOTAL SYNTHESIS OF SECURININES

A synthesis of epimeric 1-hydroxy-7-azatricyclo2.7>dodecan-9-ones (3 and 4), in ten steps from p-methoxyphenol, is described.They have been converted to the corresponding 9(10)-olefinic derivatives 22 and 23.