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Indol-3-yl-phenyl-methanone oxime is a chemical compound with the molecular formula C16H12N2O. It is derived from indole, a heterocyclic aromatic organic compound, and phenylmethanone, also known as benzoyl. The oxime functional group is formed by the addition of a hydroxylamine (NH2OH) molecule to a carbonyl group (C=O). indol-3-yl-phenyl-methanone oxime is characterized by its unique structure, which combines the properties of indole and phenylmethanone, and the presence of the oxime group, which can participate in various chemical reactions. It is used in the synthesis of pharmaceuticals and other organic compounds due to its versatile chemical properties and potential applications in drug development.

4365-74-6

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4365-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4365-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4365-74:
(6*4)+(5*3)+(4*6)+(3*5)+(2*7)+(1*4)=96
96 % 10 = 6
So 4365-74-6 is a valid CAS Registry Number.

4365-74-6Downstream Products

4365-74-6Relevant academic research and scientific papers

SELECTIVITY IN CYCLOADDITIONS-IX CYCLOADDITIONS OF NITRILE OXIDES TO INDOLES. REACTIVITY AND REGIOCHEMISTRY

Caramella, P,Corsico, A. Coda,Corsaro, A,Del Monte, D.,Albini, F. Marinone

, p. 173 - 182 (2007/10/02)

Cycloadditions of benzonitrile oxide and mesitonitrile oxide to N-methylindole and indole yield the acid sensitive cycloadducts 1 a-d with high regioselectivity.With N-carbethoxyindole the stable cycloadducts 1 e,f and minor amounts of the regioisomeric 2 e,f are isolated.The electron withdrawing substituent reduces both the regioselectivity and the reactivity of the cycloadditions.Frontier orbital considerations, based on MINDO/3 calculations, allow elucidation of the observed changes in reactivity and regiochemistry.

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