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

37904-11-3

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37904-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37904-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,0 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37904-11:
(7*3)+(6*7)+(5*9)+(4*0)+(3*4)+(2*1)+(1*1)=123
123 % 10 = 3
So 37904-11-3 is a valid CAS Registry Number.

37904-11-3Downstream Products

37904-11-3Relevant academic research and scientific papers

Synthesis of 3-chloro-1-substituted aryl pyrrolidine-2,5-dione derivatives: discovery of potent human carbonic anhydrase inhibitors

Oktay, Koray,Polat Kose, Leyla,?endil, K?v?lc?m,Gültekin, Mehmet Serdar,Gül??n, ?lhami

, p. 1619 - 1627 (2017/06/27)

Carbonic anhydrase isoenzymes are important metalloenzymes that are involved in many physiologic processes, in which they catalyze the reversible hydration of carbon dioxide (CO2) to bicarbonate (HCO3 –) and protons (Hsup

Substituent effects on the regioselectivity of maleamic acid formation and hydrogen chloride addition to N-aryl maleimides

Faturaci, Yeliz,Coskun, Necdet

, p. 749 - 758 (2013/02/25)

Itaconic anhydride reacts with aryl amines to give a substituent controlled equilibrium mixture of regioisomeric (Z)-2-methyl- and (Z)-3-methyl-4-oxo-4- (arylamino)but-2-enoic acids. Electron-donating groups favor nucleophilic attack on C-5 carbonyl, while the presence of electron-withdrawing groups enhances the bias for attack on C-2 carbonyl. The treatment of (Z)-2-methyl- and (Z)-3-methyl-4-oxo-4-(arylamino)but-2-enoic acids with SOCl2-Et 3N in THF provided the corresponding maleimides in high yields while under the same conditions the maleic anhydride aryl amine addition products gave predominately the corresponding 3-chloro-1-arylpyrrolidine-2,5-diones and maleimides in substituent dependent ratio. TUeBITAK, 2012.

α-chlorosuccinimides - A new source for maleimides and succinimides

Gǎinǎ, Constantin,Gǎinǎ, Viorica

, p. 655 - 661 (2007/10/03)

N-Arylmaleimides and N-arylsuccinimides were prepared by dehydrochlorination reaction of N-aryl α-chlorosuccinimides in the presence of a base and by reduction of 2-chlorosuccinimide in the presence of zinc, respectively. N-Aryl α-chlorosuccinimides were obtained by dehydration of N-aryl substituted maleamic acids in the presence of thionyl chloride. The structure of the synthesized compounds was confirmed by IR, 1H-NMR and 13C-NMR spectra.

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