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N-Ethylidendicyclohexylamine-oxid, also known as N-ethylidendicyclohexylamine oxide or EIC, is a chemical compound with the formula C14H27NO. It is a white crystalline solid that is widely used as a phase-transfer catalyst in various chemical reactions, particularly in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. EIC is known for its ability to facilitate the transfer of reactants between immiscible phases, such as between an aqueous and an organic phase, thereby enhancing the efficiency and selectivity of the reaction. It is also used as a surfactant and a chelating agent in various industrial applications. Due to its effectiveness and versatility, N-ethylidendicyclohexylamine-oxid plays a significant role in the field of organic chemistry and chemical engineering.

3376-30-5

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3376-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3376-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3376-30:
(6*3)+(5*3)+(4*7)+(3*6)+(2*3)+(1*0)=85
85 % 10 = 5
So 3376-30-5 is a valid CAS Registry Number.

3376-30-5Relevant academic research and scientific papers

Regiochemistry of mercury(II) oxide oxidation of unsymmetrical N,N-disubstituted hydroxylamines

Ali, Sk. Asrof,Hashmi, S. M. Azhar,Siddiqui, Mohammad N.,Wazeer, Mohammed I. M.

, p. 14917 - 14928 (2007/10/03)

Mercury(II) oxide oxidation of N,N-disubstituted hydroxylamines with the α and α' carbon atoms containing one and two hydrogen atoms, respectively, gave aldonitrones in a highly regioselective manner. Removal of the α proton is involved in the rate determining step as shown by primary kinetic isotope effect.

Synthesis and Reactions of 3-Isoxazolines

Shatzmiller, Shimon,Shalom, Eytan,Lidor, Rami,Tartkovski, Evgeni

, p. 906 - 912 (2007/10/02)

The 2-isoxazolinium salts 7, 9, 11, 13, and 18 have been prepared.Their deprotonation with trimethylamine in chloroform yielded the 3-isoxazoline derivatives 19-23.Reaction of 21 and 22 with methyl iodide in acetonitrile gave the eneammonium salts 24 and

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