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1,4-Cyclohexanedioxime is an organic compound with the chemical formula C6H10N2O2, derived from cyclohexane. It is a white crystalline solid that is soluble in water and various organic solvents. 1,4-cyclohexanedioxime is formed by the reaction of cyclohexanone with hydroxylamine, resulting in the conversion of the carbonyl group into an oxime group. 1,4-Cyclohexanedioxime is primarily used as an intermediate in the synthesis of various chemicals, such as nylon-6,6, and caprolactam, which are important components in the production of synthetic fibers and plastics. Additionally, it has applications in the pharmaceutical industry and as a reagent in analytical chemistry.

6212-72-2

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6212-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6212-72-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6212-72:
(6*6)+(5*2)+(4*1)+(3*2)+(2*7)+(1*2)=72
72 % 10 = 2
So 6212-72-2 is a valid CAS Registry Number.

6212-72-2Relevant academic research and scientific papers

Dioximate- and Bis(salicylaldiminate)-bridged titanium and zirconium alkoxides: Structure elucidation by mass spectrometry

Maurer, Christian,Pittenauer, Ernst,Puchberger, Michael,Allmaier, Guenter,Schubert, Ulrich

, p. 343 - 351 (2013)

The treatment of titanium alkoxides with 1,5-pentanedioxime or 2,5-hexanedioxime resulted in the formation of complexes [{TiL(OR) 2}2] in which the dioximate ligands (L) bridge a dimeric Ti2(μ2-OR)2 u

From 1,4-diketones to N-vinyl derivatives of 3,3′-bipyrroles and 4,8-dihydropyrrolo[2,3-f]indole in just two preparative steps

Trofimov, Boris A.,Zaitsev, Alexey B.,Schmidt, Elena Yu.,Vasil'tsov, Alexander M.,Mikhaleva, Al'bina I.,Ushakov, Igor' A.,Vashchenko, Alexander V.,Zorina, Nadezhda V.

, p. 3789 - 3791 (2007/10/03)

Dioximes of hexane-2,5-dione and cyclohexane-1,4-dione react with acetylene in an autoclave (KOH/DMSO, 100°C, 1h, initial pressure 14atm) to give 2,2′-dimethyl-1,1′-divinyl-[3,3′]bipyrrole and 1,5-divinyl-4,8-dihydropyrrolo[2,3-f]indole in 12% and 6% yiel

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