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(Z)-3-(3-bromophenylimino)indolin-2-one is a chemical compound with the molecular formula C14H9BrN2O. It is an indolin-2-one derivative, featuring a 3-bromophenyl group attached to the imino group at the 3-position. (Z)-3-(3-bromophhenylimino)indolin-2-one is characterized by its unique structure, which includes a 2-oxindole core with a double-bonded imino group and a bromine atom on the phenyl ring. It is often used in organic synthesis and medicinal chemistry, particularly in the development of potential pharmaceuticals and other bioactive molecules. The compound's properties, such as its reactivity and potential applications, are influenced by the presence of the bromine atom, which can participate in various chemical reactions, including halogenation and substitution processes.

33828-99-8

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33828-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33828-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,8,2 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33828-99:
(7*3)+(6*3)+(5*8)+(4*2)+(3*8)+(2*9)+(1*9)=138
138 % 10 = 8
So 33828-99-8 is a valid CAS Registry Number.

33828-99-8Downstream Products

33828-99-8Relevant academic research and scientific papers

Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes

Beloglazkina, Elena,Filatov, Vadim,Kukushkin, Maksim,Kuznetsova, Juliana,Majouga, Alexander,Skvortsov, Dmitry,Tafeenko, Viktor,Zyk, Nikolay

, p. 14122 - 14133 (2020)

A new synthetic approach for realizing biologically relevant bis-aryl spiro[azetidine-2,3′-indoline]-2′,4-diones was developed based on Staudinger ketene-imine cycloaddition through the one-pot reaction of substituted acetic acids and Schiff bases in the presence of oxalyl chloride and an organic base. A series of [azetidine-2,3′-indoline]-2′,4-diones were synthesized using this method. For comparison, the same compounds were obtained using a known technique, where ketene is generated from pre-synthesized acyl chloride. It was shown that the use of oxalyl chloride for ketene generation in the one-pot reaction at room temperature allows for the reversal of the diastereoselectivity of spiro-lactam formation, unlike previously described procedures.

On antimicrobial activity of 3'-phenylspiro[3H-indole-3,2'-thiazolidine]-2,4' (1H)-diones

Diurno,Mazzoni,Piscopo,Bolognese

, p. 435 - 441 (2007/10/02)

3'-substituted phenylspiro[3H-indole-3,2'-thiazolidine]-2,4' (1H)-diones (1-15), tested toward Gram-positive, Gram-negative bacteria and Fungi, showed a significant activity against Gram-positive bacteria.

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