Category: 2272-40-4

Soluble maleimide prepolymers containing 1,3,5-triazine group as composite resin matrixes. Part 1. Synthesis and characterization was written by Dolui, Swapan K.;Maiti, Sukumar. And the article was included in Journal of Polymer Materials in 1991.Recommanded Product: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Low-mol.-weight amine-terminated monomaleimide prepolymers containing 1,3,5-triazine groups were synthesized by cocondensing benzophenonetetracarboxylic dianhydride, diamines having 1,3,5-triazine groups, and maleic anhydride. These low-mol.-weight reactive prepolymers were soluble in low-boiling solvents such as CHCl₃, THF, etc. These were characterized by elemental (N) analyses, IR, and NMR spectroscopy, vapor-pressure osmometry, and viscosity. On heating at 180-190° these prepolymers underwent simultaneous chain extension by Michael addition reaction and crosslinking by mutual reaction between their amine-terminated and maleimide-terminated ends. The cured polyimides were thermally stable and their thermal behavior was studied by TGA, DTA, and isothermal aging at 200-250°. 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. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. 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.Recommanded Product: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Preparation of polyimide-cellulose composite using oligoimide with ethynyl terminals was written by Shirata, Tomoya;Kon, Tatsuki;Sasaki, Keiko;Oishi, Yoshiyuki;Shibasaki, Yuji. And the article was included in Chemistry Letters in 2014.Application of 2272-40-4 The following contents are mentioned in the article:

A soluble imide oligomer (IO) (repeating number; 2 and 4) having N-phenylated melamine units and phenylethynyl terminals was prepared, and the application to polyimide composites with cellulose (CEL) crystals derived from pulp (CEL_p) or Halocynthia (CEL_h) with or without a modifier was investigated. The CEL_h additive up to 0.5 weight % was easily dispersed in IO matrix in solution, and thermostable (glass-transition temperature, ca. 285 °C) transparent tough film (tensile strength, ca. 169 MPa; elongation at break, ca. 8.9%; tensile modulus, ca. 4.6 GPa) was obtained, while the addition of a modifier such as cetyltrimethylammonium bromide and poly(ethylene glycol) derivatives was necessary to obtain a similar tough film for the CEL_p additive. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Application of 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. 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.Application of 2272-40-4

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

Microwave-assisted synthesis of coumarin based 1,3,5-triazinyl piperazines and piperidines and their antimicrobial activities was written by Patel, Divyesh;Patel, Rahul;Kumari, Premlata;Patel, Navin. And the article was included in Acta Poloniae Pharmaceutica in 2012.Reference of 2272-40-4 The following contents are mentioned in the article:

A series of 1,3,5-triazines, containing aniline, 4-hydroxycoumarin, and 7-hydroxy-4-methylcoumarin and different piperazines or piperidines as substituents on the C atoms of the triazine ring, was synthesized by a simple and efficient synthetic protocol. Comparative studies were performed on above compounds, which were synthesized by amination with conventional and microwave heating. The microwave method was observed to be more beneficial as it provides an increase of yield and 90-95% reduction of time. The antimicrobial activity of the compounds was tested against bacteria (S. aureus, B. subtilis, E. coli, P. aeruginosa) and fungi (A. niger, C. albicans). The preliminary in vitro evaluation studies revealed that some of the compounds have promising antimicrobial activities. 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. 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. 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.Reference of 2272-40-4

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

In vitro antimicrobial assessment of coumarin-based s-triazinyl piperazines was written by Patel, Divyesh;Patel, Rahul;Kumari, Premlata;Patel, Navin. And the article was included in Medicinal Chemistry Research in 2012.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

A series of 1,3,5-triazines containing aniline, coumarins (4-hydroxycoumarin and 7-hydroxy-4-methylcoumarin), and different piperazine moieties as substituent on the C atoms of the triazine ring were synthesized by a simple and efficient synthetic protocol. Comparative studies were performed on the above series, which was prepared via amination of appropriate chlorotriazines with conventional and microwave heating. The microwave method was observed to be more beneficial as it provides an increase in yield and 90-95% reduction of time. All the synthesized compounds were examined for their efficacy against Gram -ve bacteria (E. coli and P. aeruginosa), Gram +ve bacteria (S. aureus and B. subtilis), and fungal species (C. albicans and A. niger) with an intent to overcome multiple drug resistance to the pathogenic strains. 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. 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.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Prediction of log k_w using MCIs and LSER methods for heterocyclic nitrogen compounds was written by Li, Li;Yang, Hong;Ding, Yanbing;Wang, Liansheng;Zhang, Zheng. And the article was included in Journal of Liquid Chromatography & Related Technologies in 1999.Computed Properties of C9H6Cl2N4 The following contents are mentioned in the article:

The HPLC capacity factors(k’) measured on a C₁₈ column, using methanol-water mobile phase of different compositions, were determined for 15 heterocyclic nitrogen compounds The linear relationship between the log k’ values and the percentage of the methanol in the eluent was studied for each compound The log k_w‘ values of these compounds were obtained by extrapolating the retention data in binary solvent system to pure water eluent. Various MCI’s (mol. connectivity indexes) were calculated and LSER(linear solvation energy relationship) parameters were observed for these compounds Good correlations were established between MCI’s and log k_w‘, and between LSER parameters and log k_w‘. The present correlation can be used to predict log k_w‘ values for other derivatives 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. 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.Computed Properties of C9H6Cl2N4

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

Chemical modification of cellulose to improve its transfer printability was written by Amirshahi, S. H.;Afgeh, M. Ghanbar. And the article was included in Iranian Journal of Polymer Science & Technology in 2001.Application of 2272-40-4 The following contents are mentioned in the article:

By synthesizing a reactive hydrophobe from cyanuric chloride and applying it on cellulosic (cotton) fabric, the water absorption of the fabric is decreased. This hydrophobic substance is anilinodichlorotriazine (ADTC) and is able to react with cellulose like a reactive dye. A strong covalent bond between ADTC and cellulose in the fiber leads to the blockage of hydroxyl groups and reduces the possibility of hydrogen bonding between he fibers and water. Hence, the possibility of transfer printing of treated fabric is facilitated. The relation between the printability of treated fabric with disperse dyes and the concentrations of the reactive hydrophobe is considered. Finally, by varying the inorganic/organic ratio for the treated fabric to the disperse dyes, the affinity of the dyes to cellulose is examined This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Application of 2272-40-4).

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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Application of 2272-40-4

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

Synthesis and structural-reactivity studies of bifunctional MCT/SES (monochlorotriazine/sulphatoethylsulphone) azo reactive disperse dyes applied to wool and polyester fabric was written by Eko, Ishegbe Joyce;Ademola, Bello Kasali;Obinna, Nkeonye Peter;Kogo, A. A.. And the article was included in Chemical Science International Journal in 2019.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

Reactive disperse dyes containing monochlorotriazine/sulphatoethylsulfone reactive moieties were synthesized by condensing aniline with cyanuric chloride and further reacting it with a series of monoazo dyes obtained by diazotising 1-aminobenzene-4-β-sulphatoethylsulfone and coupling with various substituted 2-amino-4-phenylthiazole derivatives The dyeing performance of the dyes was evaluated on polyester and wool fabrics. The dyes obtained gave various shades ranging from reddish to bright red colors. They had good depth and good leveling properties. They dyed fabrics showed moderate to good light fastness properties and very good to excellent fastness to washing and perspiration. The dye bath exhaustion on the polyester and wool fabrics were found to be very good and their fixation values were moderate. 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.SDS of cas: 2272-40-4

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

Room temperature liquid crystal of symmetric gallic trimer containing cyanuric core: synthesis and mesomorphism was written by Guo, Hongyu;Fang, Xiaoting;Yang, Fafu;Wu, Yamin. And the article was included in Liquid Crystals.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:

Three novel gallic monomer , dimer and trimer with conjugated cyanuric core were designed and synthesized by Schiff-base condensation mode in yields of 80-90%. Their structures were characterised by fourier transform IR spectroscopy, ¹H NMR (NMR), electrospray ionization mass spectrometry and elemental analyses. Their mesomorphic behaviors were investigated by differential scanning calorimetry, polarising optical microscopy and X-ray diffraction. The gallic monomer has no mesomorphic property, but the dimer and trimer possess good mesomorphic properties. The trimer with high symmetry exhibited the typical hexagonal columnar liquid crystal at room temperature The temperature range of mesophase is as wide as 149°C (14-163°C). The results suggested that the more gallic units and sym. structures are favorable for excellent mesomorphic properties. 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. 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.Synthetic Route of C9H6Cl2N4

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

Novel discotic liquid crystal oligomers: 1,3,5-triazine-based triphenylene dimer and trimer with wide mesophase was written by Yang, Fafu;Xie, Jianwei;Guo, Hongyu;Xu, Bingting;Li, Congcong. And the article was included in Liquid Crystals in 2012.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Series of novel 1,3,5-triazine-based triphenylene oligomers , and with large bridging polyaromatic core were designed and synthesized by simple procedures in high yields. Their structures were confirmed by FT-IR, ¹H NMR, ESI-MS and elemental analyses. Their mesomorphic behaviors were studied by differential scanning calorimetry, polarizing optical microscopy and X-ray diffraction. 1,3,5-triazine-based triphenylene monomer has no mesomorphic property, but 1,3,5-triazine-based triphenylene dimer and 1,3,5-triazine-based triphenylene trimer possess excellent mesomorphic properties. The mesomorphic temperature range of compound was as wide as 180°. These studies indicated that the mesomorphic properties were determined by the numbers of triphenylene units. More units of triphenylene in the oligomers resulted in better mesomorphic properties. 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. 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).Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Microwave assisted synthesis and in vitro antimicrobial assessment of quinolone based s-triazines was written by Patel, Divyesh;Patel, Rahul;Kumari, Premlata;Patel, Navin. And the article was included in Heterocyclic Communications in 2011.Computed Properties of C9H6Cl2N4 The following contents are mentioned in the article:

A series of 1,3,5-triazine derivatives that contain aniline, 4-hydroxy-N-methylquinolone and different piperazine and piperidine moieties as substituents on the carbon atoms of the triazine ring was synthesized by a simple and efficient synthetic protocol. Comparative studies were performed on the compounds, which were synthesized with conventional and microwave heating methods. The microwave method is more beneficial as it provides an increase in yield and 90%-95% reduction time. The antimicrobial activity of the compounds was tested against seven bacteria (Staphylococcus aureus, Bacillus cereus, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Salmonella typhi, Proteus vulgaris) and two fungi (Aspergillus niger, Candida albicans). Some of the novel s-triazines noteworthy activity in MIC and agar diffusion tests. 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. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. 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