Category: 2272-40-4

The genotoxicity of selected heterocyclic nitrogen compounds. A quantitative structure-activity relationship study was written by Zhu, C. M.;Kong, L. R.;Shen, Q. L.;Zhang, M.;Chen, J. W.;Huang, Q. G.;Wang, L. S.. And the article was included in Toxicological and Environmental Chemistry in 1998.Recommanded Product: 2272-40-4 The following contents are mentioned in the article:

The genotoxicity of heterocyclic N compounds was evaluated by micronuclei test of Vicia faba root tip cell. All these chems. are genotoxic. A meaningful Quant. Structure-Activity Relationship (QSAR) model was proposed by the quantum chem. descriptors: MN = -0.467-3.198 Elumo + 9.732q⁺. The above equation is significant because of its great RE and F values. It may reveal the mutagenic mechanism to some extent and can be used to describe the genotoxicity of 13 tested chems. The main key steps are metabolic course and mutagenic reaction. The chem. with higher q⁺ and lower Elumo has greater genotoxicity. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Recommanded Product: 2272-40-4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Recommanded Product: 2272-40-4

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Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Synthesis, structure, and dynamic behavior in solution of arylamino-1,3,5-triazines was written by Belyakov, P. A.;Shastin, A. V.;Strelenko, Yu. A.. And the article was included in Russian Chemical Bulletin in 2005.Computed Properties of C9H6Cl2N4 The following contents are mentioned in the article:

Ten unsym. substituted arylamino-1,3,5-triazines were synthesized and studied by dynamic NMR spectroscopy. The free energies of the hindered rotation are in 59-77 kJ mol^-1 range. Using difference-mode NOE NMR experiments, the structures of the major and minor rotation isomers were proved. The DFT B3LYP/6-31G* calculations were performed. The difference between the calculated rotation barriers and the exptl. values obtained by line shape anal. is less than 7.6 kJ mol^-1. The height of the rotation barrier varies in a 18 kJ mol^-1 range depending on the substituents in the triazine ring. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Computed Properties of C9H6Cl2N4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Computed Properties of C9H6Cl2N4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Quantitative structure-activity relationships and mixture toxicity studies of heterocyclic nitrogen compounds was written by Chen, J.;Liao, Y.;Zhao, Y.;Wang, L.;Lu, G.;Zhao, T.. And the article was included in Bulletin of Environmental Contamination and Toxicology in 1996.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

The toxicity of 13 heterocyclic nitrogen compounds to Daphnia magna and the resultant QSARs of these chems. based on the measured logKow values were reported. Mixture toxicities were also reported. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Erratum to: Synthesis and characterization of new s-triazine bearing benzimidazole and benzothiazole derivatives as anticancer agents [Erratum to document cited in CA163:520453] was written by Kumar, G. Jagadeesh;Kumar, S. Naveen;Thummuri, Dinesh;Adari, Lavanya Bindu Sree;Naidu, V. G. M.;Srinivas, Kolupula;Rao, V. Jayathirtha. And the article was included in Medicinal Chemistry Research in 2017.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

In the original publication, the IC₅₀ values of compounds 15f, 15g and their resp. dose response curves in Fig. 1 are incorrect; the correction is provided here. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Category: chlorides-buliding-blocks).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Category: chlorides-buliding-blocks

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Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Studies on s-triazines. Part VIII. Preparation of L (+) or (-)-2-arylamino-4,6-di-α-glutarylamino-s-triazines was written by Batt, S. B.;Khunt, V. N.;Parikh, A. R.. And the article was included in Chemical Era in 1979.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

The title triazines were prepared by acylation of 2-(arylamino)-4,6-dichloro-s-triazine with L-(+)-glutamic acid in HCl. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Synthesis of 4-amino-6-chloro-1,3,5-triazin-2(1H)-ones was written by Bakharev, V. V.;Gidaspov, A. A.;Parfenov, V. E.;Ul’yankina, I. V.;Zavodskaya, A. V.;Selezneva, E. V.;Suponitskii, K. Yu.;Sheremetev, A. B.. And the article was included in Russian Chemical Bulletin in 2012.Formula: C9H6Cl2N4 The following contents are mentioned in the article:

Conditions for selective substitution for one Cl in 2-(substituted amino)-4,6-dichloro-1,3,5-triazines with HO^– were elaborated. Spectra and calculation showed that the products formed are in the lactam form, i.e., have the structure of 4-chloro-6-(substituted amino)-1,3,5-triazin-2(1H)-ones. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Formula: C9H6Cl2N4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Formula: C9H6Cl2N4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Synthesis and application of chiral triazine condensing reagents prepared from esters of amino acids was written by Kaminski, Zbigniew J.;Zajac, Krzysztof J.;Jastrzabek, Konrad. And the article was included in Acta Biochimica Polonica in 2001.Formula: C9H6Cl2N4 The following contents are mentioned in the article:

Treatment of cyanuric chloride with chiral amines or esters of chiral amino acids gave chiral 2,4-dichloro-6-alkylamino-1,3,5-triazines (2-5) in 49-69% yield, which were found useful as coupling reagents. Enantioselective activation and enantioselective aminolysis in the presence of 2-5 was observed This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Formula: C9H6Cl2N4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Formula: C9H6Cl2N4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Synthesis and characterization of azacyclophanes of 1,3,5-triazine was written by Liu, Yanfeng;Hua, Chengwen;Gou, Xiaofeng;Zhao, Junlong. And the article was included in Youji Huaxue in 2009.Product Details of 2272-40-4 The following contents are mentioned in the article:

Several novel azacyclphanes were synthesized from cyanuric chloride, aniline, ethylamine, p-nitrophenol and di(4-aminophenyl) ether by substitution, reduction and cyclization, and their structures were characterized by ¹H NMR, IR, MALDI-TOFMS techniques and elemental anal. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Product Details of 2272-40-4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Product Details of 2272-40-4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Synthesis and properties of N-sulfomethyl-N-2-(4,6-dichlorotriazinyl)aniline was written by Pigulya, S. G.;Islyaikin, M. K.;Smirnov, R. P.. And the article was included in Izvestiya Vysshikh Uchebnykh Zavedenii, Khimiya i Khimicheskaya Tekhnologiya in 1993.Recommanded Product: 2272-40-4 The following contents are mentioned in the article:

N-(sulfomethyl)-N-2-(4,6-dichlorotriazinyl)aniline (I) was prepared by reaction of N-(sulfonylmethyl)aniline with 2,4,6-trichloro-1,3,5-triazine. The physicochem. properties of I were studied. Relative reactivities in the reaction were also studied. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Recommanded Product: 2272-40-4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Recommanded Product: 2272-40-4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Studies on s-triazines – Part VIII. Preparation of L(+) or (-)-2-arylamino-4,6-di-α-glutarylamino-s-triazines was written by Bhatt, S. B.;Khunt, V. N.;Parikh, A. L.. And the article was included in Metals and Minerals Review in 1979.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Title compounds I (R = H, Me, MeO, NO₂, Cl) were prepared by reaction of 2-(phenylamino)-4,6-dichloro-1,3,5-triazines with glutamic acid Na salt. Optical rotations of I in pyridine and aqueous NaOH were determined This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics