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2-Aziridinecarbonitrile, 1-cyclohexyl-2,3,3-trimethyl- is a complex organic chemical compound with the molecular formula C11H18N2. It is a derivative of aziridine, a heterocyclic compound containing a three-membered ring with one nitrogen atom and two carbon atoms. The compound features a cyclohexyl group attached to the 1-position, and two methyl groups at the 2 and 3 positions, along with a nitrile group (CN) at the 2-position. 2-Aziridinecarbonitrile, 1-cyclohexyl-2,3,3-trimethyl- is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to handle 2-Aziridinecarbonitrile, 1-cyclohexyl-2,3,3-trimethyl- with care, as it may have potential health risks and should be stored and used according to proper safety guidelines.

81803-22-7

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81803-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81803-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,0 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81803-22:
(7*8)+(6*1)+(5*8)+(4*0)+(3*3)+(2*2)+(1*2)=117
117 % 10 = 7
So 81803-22-7 is a valid CAS Registry Number.

81803-22-7Downstream Products

81803-22-7Relevant academic research and scientific papers

A Novel Synthesis of α-Cyanoaziridines

Kimpe, Norbert De,Moens, Luc,Verhe, Roland,Buyck, Laurent De,Schamp, Niceas

, p. 19 - 20 (1982)

A new route to α-cyanoaziridines has been developed by reaction of α-chloroketimines with potassium cyanide in methanol, which involves nucleophilic addition and subsequent intramolecular nucleophilic substitution.

STUDY OF THE INFLUENCING FACTORS ON THE REACTION OF α-HALOGENATED KETIMINES WITH CYANIDE ION

Kimpe, Norbert De,Sulmon, Paul,Schamp, Niceas

, p. 567 - 586 (2007/10/02)

The reaction of α-halogenated ketimines with cyanide ion in various solvents leads to α-cyanoaziridines.The scope and limitations of this reaction have been studied by investigating reaction parameters such as the nitrogen substituent, the solvent, the so

Formation of α-Cyanoaziridines and 1-(Alkylamino)cyclopropanecarbonitriles by Cyanation of α-Halo Ketimines

De Kimpe, Norbert,Sulmon, Paul,Verhe, Roland,De Buyck, Laurent,Schamp, Niceas

, p. 4320 - 4326 (2007/10/02)

A new convenient synthesis of α-cyanoaziridines was developed by reaction of α-halo ketimines with cyanide in methanol or acetonitrile.Tertiary α-chloro ketimines with cyanide in methanol gave rise to a competitive reaction between α-cyanoaziridine formation and production of 1-(alkylamino)cyclopropanecarbonitriles, the latter being classified as a Favorskii rearrangement-type product.The scope and limitations of this reaction have been determined by investigation of reaction parameters such as the nitrogen substituent, the solvent, the inorganic cyanide, the carbon skeleton, and the nature of the α-halogen.

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