Category: 2272-40-4

Preparation of s-triazine-Δ²-pyrazolines. I. 3,5-diphenyl-Δ²-pyrazoline reaction with chloro-s-triazines was written by Prejmereanu, Ioan;Sebe, Ion;Floru, Lucian. And the article was included in Revistade Chimie (Bucharest, Romania) in 1994.Application of 2272-40-4 The following contents are mentioned in the article:

3,5-Diphenyl-Δ²-pyrazoline (I) acylation reaction with cyanuric chloride or its mono- or di-substituted derivatives was studied, with respect to the nucleophilic reagent, acylation agent, , catalyst presence, temperature, and reaction solvent in preparation of the title compounds II (X, Y = Cl, R²R¹N, RO wherein R, R¹, R² = H, alkyl, aryl). Cyanuric chloride was reacted with I at 5° for 30 min to give II (X = Y = Cl). 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. 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.Application of 2272-40-4

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

s-Triazine derivatives and their microbial activity: Part-1 was written by Patel, R. P.;Chaudhari, J. A.;Hathi, M. V.. And the article was included in Oriental Journal of Chemistry in 2007.Formula: C9H6Cl2N4 The following contents are mentioned in the article:

Various 2-phenylamino-4,6-diphenylhydrazino-1,3,5-triazines I (Ar = Ph, ClC₆H₄, BrC₆H₄, MeC₆H₄, MeOC₆H₄, Me₂CHC₆H₄) were prepared by reaction of 2-phenylamino-4,6-dichloro-1,3,5-triazine and various phenylhydrazine derivatives I were characterized by elemental anal. and IR spectral studies. I were screened for microbial activity against Gram-pos. and Gram-neg. bacteria. 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. 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. 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.Formula: C9H6Cl2N4

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

Synthesis and bioevaluation of hybrid 4-aminoquinoline triazines as a new class of antimalarial agents was written by Kumar, Ashok;Srivastava, Kumkum;Raja Kumar, S.;Puri, S. K.;Chauhan, Prem M. S.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2008.Related Products of 2272-40-4 The following contents are mentioned in the article:

The emergence and rapid spread of chloroquine resistant strains of Plasmodium falciparum has dramatically reduced the chemotherapeutic options. Towards this goal, a series of new class of hybrid 4-aminoquinoline triazines were synthesized and screened against CQ sensitive strain 3D7 of P. falciparum in an in vitro model. Compounds I and II exhibited more than 99% suppression on day 4 and on day 6 post treatment, compound II showed impressive 99.11% suppression against CQ resistant strain N-67 of P. yoelii in an in vivo assay. 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. 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.Related Products of 2272-40-4

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

Synthesis of some novel heterocyclic azo dyes for acridine derivatives and evaluation of their antibacterial activities was written by Shihab, Nezar L.;Intedhar, K. M.. And the article was included in Journal of Chemical and Pharmaceutical Research in 2013.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Five new azo dye containing acridine derivatives (e.g., I) were synthesized using different approaches depending on the position of the functional groups. The synthesis started with unsubstituted acridine that was converted by nitration and amination to 2,9-diaminoacridine which was subjected to diazotization with (2,4-dichloro-6-triazinyl)aniline DCTA. The structures of the newly synthesized compounds were characterized by NMR, Mass, FT-IR spectra data and elemental anal. All the synthesized compounds were screened for their antibacterial activities. 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. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. 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

The configuration of N-alkyl-anilino-s-triazine derivatives was written by Wu, Zuwang;Yang, Haiyan;Sun, Zhonghai. And the article was included in Journal of Chemical Research, Synopses in 2001.Name: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

The alkyl group on the imino bridge of heterobifunctional reactive dyes plays a major role in improving the dyeing properties. The configurations of a pair of model compounds 2,4-dimethoxy-6-anilino-s-triazine and 2,4-dimethoxy-6-(N-methyl-anilino)-s-triazine have been determined by X-ray diffraction anal. of single crystals. The planar angle between the triazinyl and Ph rings of the above models are 8.35° and 72.220 resp. it indicates that the steric effect of the Et group produces a non-planar configuration and leads to the improvement of the dyeing properties. 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Name: 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Synthesis of bis(phenylamino)-1,3,5-triazine derivatives was written by Kapadia, Kishor;Solankee, Pankit;Prajapati, Yogesh;Patel, Hiral;Solankee, Sejal;Solankee, Anjani. And the article was included in Organic Chemistry: An Indian Journal in 2007.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:

A method for the synthesis of the title compounds is reported here. The title compounds thus prepared included 1-[4-[[2,4-bis(phenylamino)-1,3,5-triazin-2-yl]amino]phenyl]-1-propen-1-one derivatives and N,N’-bis(phenylamino)-N”-[4-(2-amino-3-pyrimidinyl)phenyl]-1,3,5-triazine-2,4,6-triamine and N,N’-bis(phenylamino)-N”-[4-(2,3-dihydro-1,5-benzothiazepin-4-yl)phenyl]-1,3,5-triazine-2,4,6-triamine derivatives The constitutions of newly synthesized compounds have been established on the basis of their elemental anal., IR and ¹H NMR spectral data. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Synthetic Route of C9H6Cl2N4).

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.Synthetic Route of C9H6Cl2N4

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

Synthesis, characterization and evaluation of 1,3,5-triazine aminobenzoic acid derivatives for their antimicrobial activity was written by Al-Zaydi, Khadijah M.;Khalil, Hosam H.;El-Faham, Ayman;Khattab, Sherine N.. And the article was included in Chemistry Central Journal in 2017.COA of Formula: C9H6Cl2N4 The following contents are mentioned in the article:

1,3,5-Triazines, particularly aminochlorotriazinylbenzoates and diaminotriazinylbenzoates such as I (R = PhNH, PhCH₂NH, Et₂N, 4-morpholinyl, 1-piperidinyl; R¹ = Cl, PhNH, PhCH₂NH, Et₂N, 4-morpholinyl, 1-piperidinyl; R² = H, Me) were prepared and tested for their antibacterial activities against Escherichia coli and Staphylococcus aureus and for their antifungal activities against Candida albicans. The toxicities of I (R = PhCH₂NH, 1-piperidinyl; R¹ = Cl; R² = H) were determined This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4COA of Formula: 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).COA of Formula: C9H6Cl2N4

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

Synthesis and antibacterial activity of 2-phenyl amino-4-(aryl thio ureido/aryl ureido)-6-[{4′-(2”,4”-dichloro-5”-fluoro phenyl)-6′-(3”,4”,5”-trimethoxy phenyl) pyrimidine-2′-yl}amino]-s-triazine was written by Patel, Vikram;Desai, Vikas. And the article was included in Asian Journal of Chemistry in 2003.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Some new s-triazine derivatives have been prepared by the condensation of aniline and cyanuric chloride giving 2-Ph amino-4,6-dichloro-s-triazine, which on reaction with aryl thio ureido/aryl ureido gives 2-Ph amino-4-aryl thio ureido/aryl ureido-6-chloro-s-triazine which on further reaction with 2-amino-4-(2′,4′-dichloro-5′-fluoro phenyl)-6-(3′,4′,5′-trimethoxy phenyl) pyrimidine gives the title compound The structure of the product has been characterized by elemental anal. and spectral data. The products have been screened for their antibacterial activity against Staphylococcus aureus and Escherichia coli. 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. 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).Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Synthesis, spectral and biological studies of some s-triazine derivatives of 1-(1-(4methoxyphenyl)ethyl)cyclohexanol was written by Sudani, Bhadreshkumar R.;Desai, Vikas A.. And the article was included in World Journal of Pharmaceutical Research in 2017.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

With the help of some new synthetic protocols a series of s-triazine derivatives of 1-(1-(4- methoxyphenyl)ethyl)cyclohexanol I (R¹ = Et, Ph, 4-ClC₆H₄, 2-ClC₆H₄, 2-O₂NC₆H₄; R² = 2-FC₆H₄, 3,4-F₂C₆H₃) is prepared Antibacterial and antifungal activities were evaluated for the selected synthesized derivatives Some of the compounds were found good activity against different Gram pos., Gram neg. bacterial strains and fungal stains. 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 can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. 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

Synthesis and biological evaluation of some new chalcones and their derivatives was written by Solankee, Anjani;Kapadia, Kishor;Thakor, Indrajit;Patel, Jayesh;Lad, Smruti. And the article was included in Asian Journal of Chemistry in 2004.SDS of cas: 2272-40-4 The following contents are mentioned in the article:

Novel α,β-unsaturated ketone-functionalized tris(amino)triazines I (R¹ = 4-FC₆H₄; R² = 3-ClC₆H₄, 2-O₂NC₆H₄, 2-furyl, 3-pyridyl, etc.) were synthesized by Claisen-Schmidt condensation between the Me ketone and aldehydes R²CHO. Further cyclocondensation of I with phenylhydrazine hydrochloride or thiourea in the basic medium gave pyrazolines II and mercaptopyrimidines III, resp. The products have been screened for their antibacterial activity in vitro. 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. 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).SDS of cas: 2272-40-4

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