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1H-1,2,3-Triazole-4-carboxylic acid, 1-(4-chloro-2-nitrophenyl)-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193544-96-6

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193544-96-6 Usage

Molecular structure

1H-1,2,3-Triazole-4-carboxylic acid, 1-(4-chloro-2-nitrophenyl)-5-phenylis composed of a triazole ring, a carboxylic acid group, a phenyl group, and a chloro-nitrophenyl group.

Triazole ring

A five-membered heterocyclic ring with three nitrogen atoms and two carbon atoms.

Carboxylic acid group

A functional group present in organic acids, consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) attached to the same carbon atom.

Phenyl group

A common aromatic group consisting of a six-membered ring with alternating single and double carbon-carbon bonds.

Chloro-nitrophenyl group

A potentially reactive and toxic substituent containing both a chlorine and a nitro group (-NO2) attached to a phenyl ring.

Medicinal chemistry applications

The compound has potential applications in the development of pharmaceuticals due to its unique structure and properties.

Organic synthesis

The compound can be used as a building block or intermediate in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 193544-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,5,4 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 193544-96:
(8*1)+(7*9)+(6*3)+(5*5)+(4*4)+(3*4)+(2*9)+(1*6)=166
166 % 10 = 6
So 193544-96-6 is a valid CAS Registry Number.

193544-96-6Relevant academic research and scientific papers

1,5-Diarylsubstituted 1,2,3-triazoles as potassium channel activators. VI

Biagi, Giuliana,Calderone, Vincenzo,Giorgi, Irene,Livi, Oreste,Martinotti, Enrica,Martelli, Alma,Nardi, Antonio

, p. 397 - 404 (2007/10/03)

As part of our program toward designing potassium channel openers, synthesis of a novel series of 1,5-diphenylsubstituted 1,2,3-triazoles, as potential activators of the large-conductance calcium-activated potassium channels (BK), as well as their vasorel

Synthesis of New 1,2,3-Triazolo[1,2-a]benzotriazole Derivatives or Substituted 2,3-Benzo-13a,6,6a-tetraazapentalenes. II

Biagi, Giuliana,Giorgi, Irene,Livi, Oreste,Manera, Clementina,Scartoni, Valerio,Barili, Pier Luigi

, p. 845 - 851 (2007/10/03)

This paper continues the synthesis of new 1,2,3-triazolo[1,2-a]benzotriazoles or 2,3-benzo-1,3a,6,6a-tetrazapentalenes to submit to biological assays. The derivatives were obtained by deoxycyclization reactions of appropriate nitrophenyl-1,2,3-triazole derivatives and by thermal decomposition of appropriate azidophenyl-1,2,3-triazoles (Schemes 1 and 2). Some attempts to extend these synthetic routes to the preparation of 1,2,4-triazolo[1,2-a]benzotriazoles (Scheme 3) and 1,2,3-triazolo[1,2-b]-4H-1,2,3-benzo-triazines (Scheme 4) completely failed.

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