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Spiro[2.3]hexane, 1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93714-50-2

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93714-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93714-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,1 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93714-50:
(7*9)+(6*3)+(5*7)+(4*1)+(3*4)+(2*5)+(1*0)=142
142 % 10 = 2
So 93714-50-2 is a valid CAS Registry Number.

93714-50-2Downstream Products

93714-50-2Relevant academic research and scientific papers

Synthesis and transformations of metallacycles 37. Cp2ZrCl 2-Catalyzed cycloalumination of substituted methylidenecyclopropane with Et3Al

D'Yakonov,Trapeznikova,Dzhemilev

experimental part, p. 107 - 111 (2011/08/07)

Cycloalumination of substituted methylidenecyclopropanes with Et 3Al catalyzed by Cp2ZrCl2 affords alumaspiro[2.4]heptanes in 64-92% yields.

One-pot synthesis of small spirocarbocycles through the catalytic cyclometalation reactions of unsaturated compounds

D'yakonov, Vladimir A.,Tuktarova, Regina A.,Trapeznikova, Olga A.,Khalilov, Leonard M.,Popod'ko, Natal'ya R.

experimental part, p. 20 - 33 (2011/06/21)

The mild and efficient one-pot methods to synthesize substituted spirocyclopropanes and spirocyclobutanes are reported. The elaborated procedures based on consecutive cycloalumination of methylenecyclopropanes, methylenecyclobutanes or cycloalkynes assist

Synthesis, Structure, and Reactions of Stable Titanacyclopentanes

Mashima, Kazushi,Sakai, Nozomu,Takaya, Hidemasa

, p. 2475 - 2483 (2007/10/02)

Titanacyclic compounds of the formula Cp*2Ti(CH2CH2C(CH2CHR)CH2) (5a; R=H and 5b; R=C6H5, Cp*=pentamethylcyclopentadienyl), the first stable titanacyclopentanes, have been prepared by the reaction of bis(pentamethylcyclopentadienyl)titanium-ethylene complex (3) with methylenecyclopropanes (4), and their structures were determined based on both spectroscopic data and X-ray crystallography.Complex 5b crystallized in space group P21/a (Z=4) with cell constants, a=21.832(3), b=8.580(1), c=14.759(2) Angstroem, β=96.81(1) deg, U=2744.9(6) Angstroem3 (4261 reflections, R=0.053).The reaction of 5 with carbon monoxide afforded spiroheptan-5-ones in 98percent yield.The thermal decomposition of 5 has been investigated, and possible mechanisms of the reactions have been proposed based on deuterium-labeled experiments.A novel formal reductive elimination of organic ligands giving 1-phenylspirohexane has been observed in the thermolysis of 5b.A structure-reactivity relationship has been discussed.

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