Category: 2272-40-4

NMR studies of the dynamic behavior of 2-anilino-6-chloro-4-methoxy-1,3,5-triazine in solution was written by Belyakov, P. A.;Shastin, A. V.;Strelenko, Yu. A.. And the article was included in Russian Chemical Bulletin in 2001.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

2-Anilino-6-chloro-4-methoxy-1,3,5-triazine was synthesized and studied by dynamic NMR. The activation parameters of hindered internal rotation in unsym. substituted arylamino-sym-triazine were determined for the first time. It was found that a sterically more hindered rotational isomer is thermodynamically more stable in this compound (slow-exchange NOE data). This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Application In Synthesis 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. 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. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Synthesis of chalcones, pyrazolines, amino pyrimidines and pyrimidinethiones as antibacterial agents was written by Solankee, Anjani;Patel, Jayesh. And the article was included in Indian Journal of Chemistry in 2004.Electric Literature of C9H6Cl2N4 The following contents are mentioned in the article:

2-Phenylamino-4-(3′-fluorophenylamino)-6-(4′-acetylphenyl-amino)-s-triazine on treatment with aromatic aldehydes yields chalcones, which on cyclization with hydrazine hydrate, guanidine nitrate and thiourea give the corresponding pyrazolines, amino pyrimidines and pyrimidinethiones, resp. The synthesized compounds are screened 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: 2272-40-4Electric Literature 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Electric Literature of C9H6Cl2N4

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

Study of the dependence of the reactivity of substituted dichloro-s-triazines on the nature of the substituent was written by Smirnova, O. V.;Bolmosova, V. P.;Kutepov, D. F.;Eryshev, B. Ya.. And the article was included in Zhurnal Prikladnoi Khimii in 1979.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:

Substituents having π-π, π-p, or π-p-π conjugation with the triazine ring increase its basicity and decrease its rate of nucleophilic substitution in polycondensation with bisphenol A [80-05-7]. Rate constants for the polymerization of 2-substituted 4,6-dichloro-1,3,5-triazines with bisphenol A increase in the substituent order: Ph < piperidyl < NHPh < NPh₂. 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. 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 readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Synthetic Route of C9H6Cl2N4

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

Synthesis and studies of chalcones and its cyanopyridine and acetyl pyrazoline derivatives was written by Solankee, Anjani;Patel, Ghanshyam;Solankee, Sejal. And the article was included in Rasayan Journal of Chemistry in 2008.Name: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Chalcones were achieved upon refluxing of ketone and different substituted aromatic and heterocyclic aldehydes in suitable solvent. Chalcones on cyclization with malononitrile in presence of ammonium acetate and hydrazine hydrate in presence of acetic acid give cyanopyridines and acetyl pyrazoline, resp. All the synthesized compounds were characterized by their phys. data and spectral data. 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. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. 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.Name: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Quantitative structure-activity relationship studies of selected heterocyclic nitrogen compounds was written by Chen, J.;Wang, L.;Lu, G.;Zhao, T.. And the article was included in Bulletin of Environmental Contamination and Toxicology in 1997.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Quant. structure-activity relationship studies were performed on seven 1,3,5-triazine derivatives , five pyrimidine derivatives and one pyridine derivative, used as intermediates in pesticide synthesis. Octanol/water partition coefficients and quantum chem. descriptors were used. Acute toxicity to Daphnia magna was compared to toxicity predicted by the equation of Y.H. Zhao, et al. (1979). This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Application In Synthesis 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. 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.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

QSAR study of the Photobacterium phosphoreum’s toxicity for triazines was written by Ding, Feng;Feng, Xin;Hu, Wei-xuan;Wang, Jin-ling;Zhou, Lu;Song, Wen-hua. And the article was included in Tianjin Shifan Daxue Xuebao, Ziran Kexueban in 2005.Formula: C9H6Cl2N4 The following contents are mentioned in the article:

Some parameters such as molar refractivity, frontier orbit energy, dipole moment, atom net charge of triazines were obtained by using the method of quantum-chem. calculation A primary QSAR model based on these parameters and the Photobacterium phosphoreum’s toxicity for compounds was established, the toxicity of the compounds was estimated with the model and some ideal results were gotten. 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 be used in production of: PVC, pesticides, chloromethane, teflon, insulators. 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 antibacterial activity of some new fluorosubstituted pyrazolines, isoxazolines and pyrimidines was written by Solankee, Anjani;Kapadia, Kishor;Thakor, Indrajit;Patel, Jayesh;Lad, Smruti. And the article was included in Oriental Journal of Chemistry in 2003.Related Products of 2272-40-4 The following contents are mentioned in the article:

Some fluoro substituted pyrazolines, e.g., I, isoxazolines and pyrimidines have been synthesized from chalcone on reaction with hydrazine, hydroxylamine and guanidine resp. Structure of these compounds have been established on the basis of spectral studies and elemental anal. All the synthesized compounds have been screened for their antibacterial activities against S. aureus, E. coli, S. paratyphi-A and B. subtilis. 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. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids.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

Synthesis and antibacterial screening of some new pyrazoline derivatives was written by Solankee, Anjani;Kapadia, Kishor;Solankee, Pankit;Prajapati, Yogesh;Patel, Hiral;Patel, Ghanshyam;Solankee, Sejal. And the article was included in Acta Ciencia Indica, Chemistry in 2008.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Aldol condensation of 2,4-bis(phenylamino)-6-(4′-acetylphenylamino)-s-triazine with different aromatic aldehydes gave chalcones. Cyclization of the chalcones with hydrazine gave acetylpyrazolines, e.g., I. All the synthesized compounds have been screened for their antibacterial activity. The structures of newly synthesized compounds have been established on the basis of their anal. and spectral data. 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. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. 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).Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Bis-crown ethers containing triazine ring. (III) was written by Lu, Guoyuan;Zhu, Chunsheng;Wang, Defen;Hu, Hongwen. And the article was included in Huaxue Shiji in 1990.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:

Extractions were carried out from aqueous alkali metal (potassium, rubidium) picrate solution with seven bis-crown ethers containing triazine ring in chloroform and the extraction equilibrium constants were evaluated. The results indicate that the bis-crown ethers having lipophilic substituents in triazine ring exhibit higher extractability. Two new bis-crown ethers I (R = PhNH, Pr) were prepared 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. 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).Synthetic Route of C9H6Cl2N4

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

Preparation of some 2-(arylamino)-4-[3-(2-methylphenyl)thiazolidine-2,4-dion-5-ylamino]-6-isonicotinylhydrazino-s-triazines as antibacterial and antituberculostatic agents was written by Desai, N. C.;Shukla, H. K.;Thaker, K. A.. And the article was included in Journal of the Institution of Chemists (India) in 1984.Reference of 2272-40-4 The following contents are mentioned in the article:

Treating arylaminotriazines I [R = (un)substituted Ph, PhCH₂) with 5-amino-3-(2-methylphenyl)-2,4-thiazolidinedione in Me₂CO at 35-40° gave II which were further treated with isoniazid to give III. The latter were effective against Mycobacterium tuberculosis at 0.02 mg/mL and against Staphylococcus aureus and Escherichia coli (no data). This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Reference of 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.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.Reference of 2272-40-4

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