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90226-47-4

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90226-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90226-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,2 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90226-47:
(7*9)+(6*0)+(5*2)+(4*2)+(3*6)+(2*4)+(1*7)=114
114 % 10 = 4
So 90226-47-4 is a valid CAS Registry Number.

90226-47-4Upstream product

90226-47-4Downstream Products

90226-47-4Relevant academic research and scientific papers

One-pot synthesis of cyclohexylamine and: N -aryl pyrroles via hydrogenation of nitroarenes over the Pd0.5Ru0.5-PVP catalyst

Chaudhari, Chandan,Sato, Katsutoshi,Ikeda, Yasuyuki,Terada, Kenji,Abe, Naoya,Nagaoka, Katsutoshi

, p. 9743 - 9746 (2021)

The direct synthesis of cyclohexylamine via the hydrogenation of nitrobenzene over monometallic (Pd, Ru or Rh) and bimetallic (PdxRu1-x) catalysts was studied. The Pd0.5Ru0.5-PVP catalyst was the most effective catalyst for this reaction. The catalyst can be reused and applied for the synthesis of N-aryl pyrroles and quinoxalines from nitrobenzenes.

Hydrogenation of 4-nitroacetophenone over Rh/silica

Currall, Kathryn,Jackson, S. David

, p. 59 - 63 (2014/08/18)

The hydrogenation of 4-nitroacetophenone (4-NAP) and 4-aminoacetophenone (4-AAP) was examined over rhodium/silica catalysts. The reactions were carried out using isopropanol as the solvent under a range of temperatures (303-333 K) and pressures (1-5 barg). An activation energy of 50 ± 4 kJ mol -1 was determined for 4-NAP hydrogenation and 48 ± 2 kJ mol-1 for 4-AAP hydrogenation. Orders of reaction were obtained for 4-NAP (zero order) and hydrogen (first order) and a kinetic isotope effect of 3.0 was observed for 4-NAP hydrogenation and ~1.4 for 4-AAP hydrogenation when deuterium was used. Under specific conditions high yields (~94%) to 4-aminoacetophenone and 1-(4-aminophenyl) ethanol could be obtained from 4-NAP hydrogenation. An antipathetic metal crystallite particle size effect was observed for both reactants.

METHOD FOR PRODUCING CYCLOHEXYL ALKYL KETONES

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Page/Page column 6, (2012/07/27)

Provided is an industrially superior method for producing cyclohexyl alkyl ketones, which solves the problems in process reduction and in disposal of wastes such as metals. An aromatic ketone represented by a formula (1) is nuclear-hydrogenated with pressurized hydrogen and in the presence of a solvent at a temperature of from 20 to 120° C., in the presence of a catalyst that carries from 0.1 to 20% by weight of a ruthenium atom on the carrier, thereby producing a cyclohexyl alkyl ketone represented by a formula (2): provided that, in the formula (2), n indicates an integer of from 1 to 3; R represents a hydroxyl group, a cyclohexyl group, an alkyl group having from 1 to 4 carbon atoms, or an acyl group having from 1 to 4 carbon atoms

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