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1,4-Piperazinedicarboximidic acid, N,N'-bis(trichloroacetyl)-, bis(2,4,6-trichlorophenyl) ester is a complex organic compound with the chemical formula C20H12Cl12N4O4. It is derived from 1,4-piperazinedicarboximidic acid, a cyclic amine with two carboxyl groups, and is characterized by the presence of two trichloroacetyl groups attached to the nitrogen atoms of the piperazine ring. The compound is further esterified with two 2,4,6-trichlorophenyl groups, which are phenyl rings substituted with three chlorine atoms at the 2, 4, and 6 positions. 1,4-Piperazinedicarboximidic acid, N,N'-bis(trichloroacetyl)-, bis(2,4,6-trichlorophenyl) ester is known for its potential applications in chemical research and as a reagent in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure and the presence of multiple chlorine atoms, it is important to handle 1,4-Piperazinedicarboximidic acid, N,N'-bis(trichloroacetyl)-, bis(2,4,6-trichlorophenyl) ester with care, as it may have specific safety and environmental considerations.

90234-99-4

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90234-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90234-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90234-99:
(7*9)+(6*0)+(5*2)+(4*3)+(3*4)+(2*9)+(1*9)=124
124 % 10 = 4
So 90234-99-4 is a valid CAS Registry Number.

90234-99-4Downstream Products

90234-99-4Relevant academic research and scientific papers

Synthesis of New Carboximidoyl Chlorides and Their Reaction with Nucleophiles

Ried, Walter,Kuembel, Brigitte,Tauer, Marie-Luise

, p. 564 - 575 (2007/10/02)

One-step reactions of N,N-dialkylcyanamides 1a-c and dicarbonitriles 1d, e with organic acyl chlorides and with 2-chloro-1,1-dicyanoethylenes easily lead to the N-acyl-substituted carboximidoyl chlorides 2a-k and biscarboximidoyl chlorides 2l-v, respectively.The substituents in the α-position of the chlorocarbonyl group have a strong influence on the stability of the reaction products.The carboximidoyl chlorides 2a, f, o, and u react with O-nucleophiles (H2O, alcohols, phenols), S-nucleophiles (dithiocarbamates, thiophenols), and N-nucleophiles (NH3, aliphatic and aromatic amines) to give a variety of products.

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