18164-50-6

Upstream product

• 105-39-5 chloroacetic acid ethyl ester 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 50-29-3 p,p'-DDT 
• 72-55-9 1,1-bis(4-chlorophenyl)-2,2-dichloroethylene 
• 23349-12-4 4,4'-(2-bromoethene-1,1-diyl)bis(chlorobenzene) 
• 2642-81-1 1,1-bis(p-chlorophenyl)ethene 
• 2642-82-2 2,2-bis(p-chlorophenyl)ethanol 
• 1774-47-6 trimethylsulfoxonium iodide 
• 104-88-1 4-chlorobenzaldehyde 
• 24337-12-0 2-(4,4'-dichloro-benzhydryl)-[1,3]dioxolane 
• 34132-11-1 2,2-bis-(p-chlorophenyl)-1-nitroethylene 
• 39479-29-3 C₃₁H₂₈Cl₂O₂ 
• 37580-81-7 1,2-bis(4-chlorophenyl)-1,2-ethandiol 
• 87413-09-0 Dess-Martin periodane 

Downstream Products

• 2642-82-2 2,2-bis(p-chlorophenyl)ethanol 
• 75057-04-4 C₃₀H₂₄Cl₂O₂ 
• 92907-72-7 N-Methyl-N'-<2,2-bis-(4-chlor-phenyl)-vinyl>-harnstoff 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 857531-24-9 4-[2,2-bis-(4-chloro-phenyl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester 
• 209159-20-6 1-[2,2-(4,4'-dichlorodiphenyl)ethyl]-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine 
• 1446743-95-8 4,4'-(3-methylbut-2-ene-1,1-diyl)bis(chlorobenzene) 
• 1333480-63-9 C₂₅H₂₀Cl₂ 
• 1333480-62-8 5-chloro-1-(4-chlorophenyl)-2-(2-methylprop-1-en-1-yl)-3-phenyl-1H-indene 
• 1333480-53-7 1,1'-(5-methyl-1-phenylhex-4-en-1-yne-3,3-diyl)bis(4-chlorobenzene) 
• 86310-29-4 C₁₅H₁₄Cl₂O₂ 

Relevant academic research and scientific papers

A gold catalytic pinacone method of rearrangement of

The invention provides a method used for catalytic rearrangement of pinacol with gold. A reaction general formula is disclosed in the invention, wherein R1, R2, R3, and R4 may be common alkyl, cycloalkyl, and aromatic rings. A gold catalyst needed by reac

PHARMACEUTICAL COMBINATIONS COMPRISING PYRAZOLE DERIVATIVES AS PROTEIN KINASE MODULATORS

The invention provides a combination comprising an ancillary compound (e.g. one, two or more ancillary compounds) and a compound of the formula (I) having protein kinase B inhibiting activity: wherein A is a saturated hydrocarbon linker group containing f

Tandem pinacol coupling-rearrangement of aromatic aldehydes with hydrogen catalyzed by a combination of a platinum complex and a polyoxometalate

Together with a strongly oxidizing polyoxometalate, H5PV 2Mo10O40, PtII(N-(2,6- diisopropylphenyl)pyrazin-2-ylmethanimine)Cl2 forms a combined catalyst that was active in the tandem pinacol coupling-rearrangement of aryl aldehydes to give mostly the corresponding diarylacetaldehyde in high yields using molecular hydrogen as the reducing agent. The Royal Society of Chemistry.

PHARMACEUTICAL COMPOUNDS

The invention provides compounds of the formula (I) having ROCK kinase and/or protein kinase p70S6K inhibiting activity: wherein A is a saturated hydrocarbon linker group containing from 1 to 7 carbon atoms, the linker group having a maximum chain length

Use of tetrahydropyridine derivatives to prepare medicines for treating diseases causing demyelination

The invention relates to the use of tetrahydropyridine derivatives of the formula in which: R1is a halogen or a CF3, (C1-C4)alkyl or (C1-C4)alkoxy group; Y is a nitrogen atom or a CH group;

Use of 4-substituted tetrahydropyridines for making medicines acting on TGF-β1

The invention relates to the use of a compound of formula (I): for the preparation of pharmaceutical compositions for increasing the circulating, cellular and extracellular levels of TGF-β1.

Electrolytic Dechlorination of DDT In a Bicontinuous Microemulsion

Electrolytic reduction in a bicontinuous microemulsion of surfactant, oil, and water removed aliphatic and aromatic chlorines from DDT. Microemulsions of didodecyldimethylammonium bromide/dodecane/water used with graphite felt cathodes provided a less expensive, less toxic approach to DDT electrolysis compared to using conventional organic solvents and metal electrodes. Good rates of aliphatic dechlorination were achieved by applying -1 V vs. Ag/AgBr and using the catalyst Co(bpy)32+, but the best yield (34 percent in 3 hr) of the fully dechlorinated hydrocarbon 1,1-diphenylethane was achieved by using -2 V with oxygen in the reaction medium.

One-pot conversion of α-substituted arylacetaldehydes into α-dicarbonyl compounds

α-dicarbonyl compounds 7-12 can be easily prepared by reaction of methylene chloride solutions of several α-substituted arylacetaldehydes 1-6 with a slight excess of tris-(o,p-dibromophenyl) ammoniumyl hexachloro antimonate A.

Reduction of 2,2-Diaryl-1-nitroethylenes : New Synthesis of 2,2-Diarylacetaldehydes and 1,1,4,4-Tetraarylbuta-1,3-dienes

2,2-Diarylacetaldehydes (VII) have been obtained by selective and controlled reduction of 2,2-diaryl-1-nitroethylenes (IV) in acid medium, and also by acid hydrolysis of 2,2-diarylvinyl-N-acetamides (VI).Nitroalkenes (IV) have been prepared by the reaction of 2,2-diarylethylenes (I) with nitrous acid whereas N-acetamide derivatives (VI) have been obtained by reductive acetylation of the nitro compounds (IV).A number of 1,1,4,4-tetraarylbuta-1,3-dienes (XI) have been obtained by the condensation of 2,2-diarylacetaldehydes (VII) with appropriate 2,2-diarylethylenes (I).Structures of the products have been assigned on the basis of analytical data and chemical and spectral evidences.