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Di-(4-chlorophenyl)maleonitrile, also known as DDD or TDE, is an organochlorine compound that was once widely used as an insecticide. It is a white crystalline solid with the chemical formula C14H8Cl2N2. DDD is a derivative of diphenylmethane, with two chlorine atoms attached to the phenyl rings and a maleonitrile group replacing the central carbon atom. This chemical was primarily used in agriculture to control pests and in household applications for termite control. However, due to its persistence in the environment and potential health risks, including endocrine disruption and carcinogenicity, its use has been largely phased out or banned in many countries. The chemical's properties, such as its lipophilicity and resistance to degradation, contributed to its environmental persistence and bioaccumulation in the food chain.

4591-17-7

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4591-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4591-17-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4591-17:
(6*4)+(5*5)+(4*9)+(3*1)+(2*1)+(1*7)=97
97 % 10 = 7
So 4591-17-7 is a valid CAS Registry Number.

4591-17-7Downstream Products

4591-17-7Relevant academic research and scientific papers

Intermolecular interactions-photophysical properties relationships in phenanthrene-9,10-dicarbonitrile assemblies

Afanasenko, Anastasiia M.,Novikov, Alexander S.,Chulkova, Tatiana G.,Grigoriev, Yakov M.,Kolesnikov, Ilya E.,Selivanov, Stanislav I.,Starova, Galina L.,Zolotarev, Andrey A.,Vereshchagin, Anatoly N.,Elinson, Michail N.

, (2020)

Phenanthrene-9,10-dicarbonitriles show various luminescence behaviour in solution and in the solid state. Aggregation patterns of phenanthrene-9,10-dicarbonitriles govern their luminescent properties in the solid state. Single crystal structures of phenan

Spectral-Fluorescence Properties of Zn(II)-Octaphenyltetraazaporphyrins

Dmitrieva, Olga A.,Chizhova, Natalya V.,Rusanov, Alexey I.,Koifman, Mikhail O.,Mamardashvili, Nugzar Z.

, p. 657 - 664 (2020)

Zn(II)-octa-(4-chlorophenyl)- and Zn(II)-octa-(4-bromophenyl)tetraazaporphyrins were synthesized by the reaction of cyclotetramerization of di-(4-chlorophenyl)- and di-(4-bromophenyl)maleonitriles with zinc(II) chloride. The obtained compounds were identi

Metal-Cocatalyst Interaction Governs the Catalytic Activity of MII-Porphyrazines for Chemical Fixation of CO2

Leal, Julia P. S. C.,Bezerra, Werberson A.,Das Chagas, Rafael P.,Franco, Chris H. J.,Martins, Felipe T.,Meireles, Alexandre M.,Antonio, Felipe C. T.,Homem-De-Mello, Paula,Tasso, Thiago T.,Milani, Jorge L. S.

, p. 12263 - 12273 (2021/08/20)

Chemical fixation of CO2 to produce cyclic carbonates can be a green and atomic efficient process. In this work, a series of porphyrazines (Pzs) containing electron-withdrawing groups and central MII ions (where M = Mg, Zn, Cu, and Co) were synthesized an

Photobleaching Efficiency Parallels the Enhancement of Membrane Damage for Porphyrazine Photosensitizers

Tasso, Thiago T.,Schlothauer, Jan C.,Junqueira, Helena C.,Matias, Tiago A.,Araki, Koiti,Liandra-Salvador, érica,Antonio, Felipe C. T.,Homem-De-Mello, Paula,Baptista, Mauricio S.

supporting information, p. 15547 - 15556 (2019/10/11)

Photostability is considered a key asset for photosensitizers (PS) used in medical applications as well as for those used in energy conversion devices. In light-mediated medical treatments, which are based on PS-induced harm to diseased tissues, the photoinduced cycle of singlet oxygen generation has always been considered to correlate with PS efficiency. However, recent evidence points to the fundamental role of contact-dependent reactions, which usually cause PS photobleaching. Therefore, it seems reasonable to challenge the paradigm of photostability versus PS efficiency in medical applications. We have prepared a series of Mg(II) porphyrazines (MgPzs) having similar singlet oxygen quantum yields and side groups with different electron-withdrawing strengths that fine-tune their redox properties. A detailed investigation of the photobleaching mechanism of these porphyrazines revealed that it is independent of singlet oxygen, occurring mainly via photoinduced electron abstraction of surrounding electron rich molecules (solvents or lipids), as revealed by the formation of an air-stable radical anion intermediate. When incorporated into phospholipid membranes, photobleaching of MgPzs correlates with the degree of lipid unsaturation, indicating that it is caused by an electron abstraction from the lipid double bond. Interestingly, upon comparing the efficiency of membrane photodamage between two of these MgPzs (with the highest and the lowest photobleaching efficiencies), we found that the higher the rate of PS photobleaching the faster the leakage induced in the membranes. Our results therefore indicate that photobleaching is a necessary step toward inflicting irreversible biological damage. We propose that the design of more efficient PS for medical applications should contemplate contact-dependent reactions as well as strategies for PS regeneration.

A two-cyano diaryl ethylene synthetic method of the compound (by machine translation)

-

Paragraph 0029-0032, (2018/07/10)

The present invention discloses a two-cyano diaryl ethylene compound synthetic methods, the method in the air atmosphere, in order to replace the benzyl cyanide as raw materials, to Ru/C, K2 CO3 As the catalyst, in ortho-dichlorobenz

Structures and photophysical properties of 3,4-diaryl-1H-pyrrol-2,5-diimines and 2,3-diarylmaleimides

Afanasenko, Anastasiia M.,Boyarskaya, Dina V.,Boyarskaya, Irina A.,Chulkova, Tatiana G.,Grigoriev, Yakov M.,Kolesnikov, Ilya E.,Avdontceva, Margarita S.,Panikorovskii, Taras L.,Panin, Andrej I.,Vereshchagin, Anatoly N.,Elinson, Michail N.

, p. 554 - 561 (2017/06/20)

Structural features of 3,4-diaryl-1H-pyrrol-2,5-diimines and their derivatives have been studied by molecular spectroscopy techniques, single-crystal X-ray diffraction, and DFT calculations. According to the theoretical calculations, the diimino tautomeri

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