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Z-C-phenyl N-(4-chlorophenylcarbamoyl) nitrone is a complex organic compound with the molecular formula C14H11ClN2O2. It is characterized by a nitrone functional group, which consists of a carbon-nitrogen double bond and a hydroxyl group attached to the nitrogen. The molecule features a phenyl ring (C6H5) at the Z-configuration, indicating the geometric arrangement of the double bond, and a 4-chlorophenylcarbamoyl group, which is a derivative of carbamic acid with a 4-chlorophenyl substituent. Z-C-phenyl N-(4-chlorophenylcarbamoyl) nitrone is of interest in the field of chemistry, particularly in the study of free radicals and as a potential building block for more complex molecules. It may also have applications in the development of pharmaceuticals or materials science due to its unique structure and reactivity.

84816-15-9

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84816-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84816-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,1 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84816-15:
(7*8)+(6*4)+(5*8)+(4*1)+(3*6)+(2*1)+(1*5)=149
149 % 10 = 9
So 84816-15-9 is a valid CAS Registry Number.

84816-15-9Relevant academic research and scientific papers

MECHANISM OF THE CARBAMOYLATION OF OXIMES

Tashchi, V. P.,Rukasov, A. F.,Orlova, T. I.,Ivanov, A. P.,Tashchi, O. A.,et al.

, p. 899 - 907 (2007/10/02)

N-Acylnitrones are formed initially during the cabamoylation of oximes of the aldehydes and ketone series.Depending on the structure of the initial compounds they can then either rearrange to O-carbamoylated oximes or undergo decomposition to N-hydroxyureas and the corresponding aldehydes and ketones.In some cases isomerization of the oximes is observed under the influence of isocyanate.

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