Category: 2272-40-4

Prediction and QSAR analysis of toxicity to Photobacterium phosphoreum for a group of heterocyclic nitrogen compounds was written by Xu, S.;Li, L.;Tan, Y.;Feng, J.;Wei, Z.;Wang, L.. And the article was included in Bulletin of Environmental Contamination and Toxicology in 2000.Recommanded Product: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

The properties of heterocyclic nitrogen compounds (partition coefficient, linear solvation energy relationship, mol. connectivity indexes, and quantum chem. descriptors) and the inhibition of bioluminescence in Photobacterium phosphoreum are explored. 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: 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. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Recommanded Product: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Reactions of aniline in acetic acid solutions containing cyanuric chloride and hydrogen chloride acceptors was written by Kolmakov, Kirill A.. And the article was included in Canadian Journal of Chemistry in 2007.Recommanded Product: 2272-40-4 The following contents are mentioned in the article:

Two reaction pathways in acetic acid solution containing cyanuric chloride, aniline, and some hydrogen chloride acceptors (triethylamine, sodium acetate, pyridine) were studied. Both aryl amination and acylation can be performed with high yields under proper reaction conditions. Contrary to the only known literature report on the reactions between carbonic acids and cyanuric chloride in the presence of a hydrogen chloride acceptor (triethylamine), it was established that acid chlorides are not formed. A scheme involving the replacement of chlorine atoms by acetate ion in the initial stage was proposed for the acylation of aniline promoted by cyanuric chloride. 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Recommanded Product: 2272-40-4

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

Modeling acute toxicity of chemicals to Daphnia magna: a probabilistic neural network approach was written by Kaiser, Klaus L. E.;Niculescu, Stefan P.. And the article was included in Environmental Toxicology and Chemistry in 2001.Related Products of 2272-40-4 The following contents are mentioned in the article:

A methodol. based on probabilistic neural networks (PNNs) is applied to model the acute toxicity (48-h LC50) of a set of 700 highly diverse chems. to Daphnia magna. First, cross-validation experiments confirming the potential use of the PNN as modeling tool for the problem at hand were performed. Next, various approaches to construct-improved models are presented. The resulting four models are then validated using an external test set of 76 addnl. compounds Input to the PNNs is derived solely from simple mol. descriptors and structural fragments and excludes bulk property parameters, such as the water solubility or the octanol/water partition coefficient This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Related Products of 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 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. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Related Products of 2272-40-4

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

Synthesis of some new penicillin and cephalosporin derivatives of substituted S-triazine and their biological activity was written by Shabadi, C. V.;Shelar, M. A.;Shelar, A. R.. And the article was included in Indian Drugs in 1998.Name: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Some new s-triazine derivatives having penicillin and cephalosporin moiety have been synthesized by the condensing monosubstituted cyanuric chlorides I [R = NHPh, NHCH₂Ph, NHC₆H₄Cl, NHC₆H₄Me, (2-methyl-1,3,4-thiadiazol-5-yl)thio, pyridin-1-yl, (3,5,6-trichloropyridin-2-yl)oxy, NHAc] with 6-aminopenicillanic acid (II), 7-aminodesacetoxycephalosporanic acid (III; R¹ = Me), and 7-aminocephalosporanic acid (III; R¹ = CH₂OAc), characterized by spectral data and are evaluated for biol. activity. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Name: 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. 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 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.Name: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

A simple and convenient synthesis of 5-amino-substituted tetrazolo[1,5-a]-1,3,5-triazin-7-one salts was written by Parfenov, Victor E.;Bakharev, Vladimir V.;Zavodskaya, Anna V.;Selezneva, Eugenia V.;Gidaspov, Alexander A.;Suponitsky, Kyrill Yu.. And the article was included in Tetrahedron Letters in 2014.Related Products of 2272-40-4 The following contents are mentioned in the article:

A simple and convenient three-step synthesis of 5-amino-substituted tetrazolo[1,5-a]-1,3,5-triazin-7-one sodium salts I (NR¹R² = NH₂, NMe₂, NHPr-n, NHPr-iso, cyclohexyl, NHPh, NHC₆H₄Me-4, pyrrolidino, piperidino, morpholino) based on a fairly simple sequence of nucleophilic substitution of chlorine atoms in cyanuric chloride has been developed. The corresponding tetrabutylammonium salts were synthesized by cation-exchange with tetrabutylammonium chloride. The structures of the products were characterized by IR, ¹H NMR and ¹³C NMR spectroscopy, and by elemental and X-ray anal. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Related Products of 2272-40-4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations.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.Related Products of 2272-40-4

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

4-Anilinoquinoline triazines: a novel class of hybrid antimalarial agents was written by Kumar, Ashok;Srivastava, Kumkum;Raja Kumar, S.;Siddiqi, M. I.;Puri, Sunil K.;Sexana, Jitendra K.;Chauhan, Prem M. S.. And the article was included in European Journal of Medicinal Chemistry in 2011.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

A novel class of hybrid 4-anilinoquinoline triazines have been synthesized and evaluated in vitro for their antimalarial activity against CQ-sensitive 3D7 strain of P. falciparum as well as for their cytotoxicity toward VERO cell line. Five compounds exhibited the antimalarial potency superior to CQ. Compounds I and II were found to be orally active at a dose of 100 mg/kg × 4 days against CQ-resistant strain of P. yoelii. Inhibition of β-hematin formation assay and mol. docking study has been conducted in order to gain insight into the mechanism of action of proposed targets for the 4-anilinoquinoline and triazine moiety of the hybrid compounds This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4SDS of cas: 2272-40-4).

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. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.SDS of cas: 2272-40-4

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

Synthesis of some new S-triazine based chalcones and their derivatives as potent antimicrobial agents was written by Solankee, Anjani;Kapadia, Kishor;Ciric, Ana;Sokovic, Marina;Doytchinova, Irini;Geronikaki, Athina. And the article was included in European Journal of Medicinal Chemistry in 2010.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:

Base-catalyzed condensation of a ketone with different aldehydes gave chalcones, 2.4-bis-(phenylamino)-6-[4′-{3”-(4”’-substituted phenyl/2”’-furanyl/2”’-thienyl)-2”-propenon-1”-yl}phenylamino]-s-thriazines. The chalcones on cyclization with hydrazine hydrate in the presence of glacial acetic acid, guanidine nitrate in the presence of alkali and malononitrile in the presence of ammonium acetate give the corresponding acetylpyrazolines, aminopyrimidines, e.g., I (R = Cl, NO₂), and cyanopyridines, resp. All the four series of products were fully characterized by spectroscopic and elemental anal., and also tested for their antibacterial activity. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Synthetic Route of 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Synthetic Route of C9H6Cl2N4

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

Synthesis of pyrazolines, isoxazolines, and aminopyrimidines as biological potent agents was written by Solankee, Anjani;Thakor, Indrajit. And the article was included in Indian Journal of Chemistry in 2006.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

Chalcones, 2-(phenylamino)-4-(4-fluorophenylamino)-6-[4-(3-aryl-1-oxoprop-2-enyl)phenylamino]-s-triazines were prepared from 4-[4-(4-fluorophenylamino)-6-(phenylamino)-1,3,5-triazin-2-yl]acetophenone. These chalcones give the corresponding pyrazolines, isoxazolines, and aminopyrimidines on cyclization with N₂H₄.H₂O, NH₂OH.HCl, and guanidine nitrate, resp. Antimicrobial activities of all synthesized compounds were screened by the cupplate method against bacteria and by the poisoned food technique against fungi. The constitutions of newly synthesized compounds were established by elemental anal., IR, and ¹H NMR. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4SDS of cas: 2272-40-4).

4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.SDS of cas: 2272-40-4

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

Synthesis and structure-activity study of fungicidal anilinopyrimidines leading to mepanipyrim (KIF-3535) as an anti-Botrytis agent was written by Nagata, Toshihiro;Masuda, Katsumi;Maeno, Shinichiro;Miura, Ichiro. And the article was included in Pest Management Science in 2004.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

A series of 2-anilinopyrimidines was prepared and their fungicidal activities against Botrytis cinerea were examined The activity fell sharply with any substitution on the anilinobenzene ring. Substitutions at the 5-position of the pyrimidine ring greatly reduced the activity. Substituents such as chloro, methoxy, methylamino, Me or 1-propynyl were well tolerated at the 4- and 6-positions of the pyrimidine ring. Among these substituents, the combination of Me and 1-propynyl groups was the most favorable. 2-Anilino-4-methyl-6-(1-propynyl)pyrimidine (KIF-3535), which showed excellent activity and no significant phytotoxicity, was finally selected for development and has been given the common name mepanipyrim. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4SDS of cas: 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.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.SDS of cas: 2272-40-4

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

Synthesis and antibacterial activity of 2-(2-carbamoylphenoxy)-4-anilino-6-phenylureido-s-triazines was written by Desai, K. R.;Pathak, M. M.. And the article was included in Journal of the Indian Chemical Society in 1985.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

Title compounds I (R = H, o-Me, m-Me, p-Me, p-NO₂, p-Cl, etc.) were prepared in 69-82% yield by treating the chlorotriazine II with RC₆H₄NHCONH₂ and aqueous NaOH in Me₂CO or dioxane. By the cup-plate method I (R = H) and I (R = o-Me) showed zones of inhibition against Staphylococcus aureus of 2.5 and 2 mm resp. By the same method against Escherichia coli, I (R = m-Me) and I (R = p-NO₂) showed zones of inhibition of 3 and 2 mm resp. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4SDS of cas: 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.SDS of cas: 2272-40-4

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