Tag: 200-300

The prediction of soil sorption coefficients of heterocyclic nitrogen compounds by octanol/water partition coefficient, water solubility, and by molecular connectivity indices was written by Liao, Y. -Y.;Wang, Z. -T.;Chen, J. -W.;Han, S. -K.;Wang, L. -S.;Lu, G. -Y.;Zhao, T. -N.. And the article was included in Bulletin of Environmental Contamination and Toxicology in 1996.HPLC of Formula: 2272-40-4 The following contents are mentioned in the article:

Soil sorption coefficients of 7 1,3,5-triazines, 4 pyrimidines, and 1 pyridazine were poorly correlated with water solubility or lipophilicity. The 1st-order mol. connectivity index was a better mol. descriptor than were solubility or lipophilicity for prediction of soil sorption coefficients of heterocyclic nitrogen compounds This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4HPLC of Formula: 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. 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).HPLC of Formula: 2272-40-4

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

Rubber/copper bonding by the use of triazine compounds was written by Anonymous. And the article was included in Research Disclosure in 1977.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

The bonding of rubber to brass-coated tire cord is improved by addition to the rubber vulcanization composition of a triazine derivative Thus, natural rubber containing conventional vulcanization additives and 2 phr 2-dimethylamino-4,6-dichloro-s-triazine (I) [2401-64-1] gave a vulcanizate with the cord-rubber bonding stregnth 60 kg, compared with 46 kg for a vulcanizate not containing I. 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Application In Synthesis of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

4,4-Disubstituted cyclohexylamine based CCR5 chemokine receptor antagonists as anti-HIV-1 agents was written by Duan, Maosheng;Aquino, Christopher;Dorsey, George F.;Ferris, Robert;Kazmierski, Wieslaw M.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2009.Recommanded Product: 53250-84-3 The following contents are mentioned in the article:

A series of 4,4-disubstituted cyclohexylamine based CCR5 antagonists has been designed and synthesized. The prepared derivatives contain arylsulfonamides and differentially linked (benzimidazolyl)azabicyclooctane moieties. Their antiviral structure-activity relationship has been extensively explored, and compound I was found to be most potent of the antagonists studied. This study involved multiple reactions and reactants, such as 2-Chloro-4-sulfamoylbenzoic acid (cas: 53250-84-3Recommanded Product: 53250-84-3).

2-Chloro-4-sulfamoylbenzoic acid (cas: 53250-84-3) 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. 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: 53250-84-3

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

Synthesis of unsymmetrical pincer CNN palladium complex of 8-dimethylamino-3-ferrocenylmethyl-3-azabicyclo[3.2.1]octane and its catalytic activity in the Suzuki reaction was written by Bulygina, Ludmila A.;Khrushcheva, Natalya S.;Lyssenko, Konstantin A.;Peregudov, Alexander S.. And the article was included in Mendeleev Communications in 2022.Safety of Sodium tetrachloropalladate(II) The following contents are mentioned in the article:

New bicyclic unsym. CNN Pd 5,6-membered pincer complex was synthesized from 3-ferrocenylmethyl-8-dimethylamino-3-azabicyclo[3.2.1]octane by its direct cyclo-palladation with Li₂PdCl₄ or Na₂PdCl₄ and NaOAc in MeOH. The obtained complex exhibited high catalytic activity in the Suzuki cross-coupling between aryl bromides and phenylboronic acid. This study involved multiple reactions and reactants, such as Sodium tetrachloropalladate(II) (cas: 13820-53-6Safety of Sodium tetrachloropalladate(II)).

Sodium tetrachloropalladate(II) (cas: 13820-53-6) 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. 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.Safety of Sodium tetrachloropalladate(II)

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

Synthesis and characterization of some novel isoxazoles and 1,5-benzothiazepines bearing s-triazine nucleus was written by Solankee, Anjani;Kapadia, Kishor;Solankee, Pankit;Prajapati, Yogesh;Patel, Hiral;Solankee, Sejal. And the article was included in Indian Journal of Chemistry in 2008.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

The title compounds were prepared starting from chalcones having s-triazine nucleus. These chalcones on cyclization with hydroxylamine hydrochloride in presence of alkali and 2-aminothiophenol in presence of a few drops of glacial acetic acid gave isoxazoles and 1,5-benzothiazepines, resp. All the products were characterized by elemental anal., IR, ¹H NMR and LCMS data. 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. 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.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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

Synthesis of new cyanomethyl-1,3,5-triazine derivatives was written by Kim, Jung-Hwan;Kim, Un-Ju. And the article was included in Journal of the Korean Chemical Society in 1996.HPLC of Formula: 2272-40-4 The following contents are mentioned in the article:

New cyanomethyl-1,3,5-triazine derivatives [I; R, R¹ = H, Pr, iso-Pr, Ph] were prepared in 78-87% yields by reaction of chloro-1,3,5-triazine derivatives with tert-Bu cyanoacetate and NaH in DMF. The intermediate (di)amino derivatives were prepared by amination of 2,4,6-trichloro-1,3,5-triazine as well as 4,6-dichloro-1,3,5-triazine derivatives This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4HPLC of Formula: 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. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.HPLC of Formula: 2272-40-4

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

Potential antitumor agents. 14. Acridylmethanesulfonanilides was written by Cain, Bruce F.;Seelye, Ralph N.;Atwell, Graham J.. And the article was included in Journal of Medicinal Chemistry in 1974.Safety of 2-Chloro-4-sulfamoylbenzoic acid The following contents are mentioned in the article:

A series of 74 structural variants of 4′-(9-acridinylamino)methanesulfonanilide hydrochloride (I) [35440-46-1] was prepared by coupling of the appropriate chloroheterocycle with a p-aminosulfonanilide. In tests in mice, 13 compounds provided some indefinite survivors of i.p. inoculation of L 1210 leukemia. Activity in relation to structure and lipophilicity was discussed. This study involved multiple reactions and reactants, such as 2-Chloro-4-sulfamoylbenzoic acid (cas: 53250-84-3Safety of 2-Chloro-4-sulfamoylbenzoic acid).

2-Chloro-4-sulfamoylbenzoic acid (cas: 53250-84-3) 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. 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).Safety of 2-Chloro-4-sulfamoylbenzoic acid

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

Silver Triflate Catalyzed Synthesis of Isoquinolino[2,1-a]quinazolino[3,2-c]quinazoline Derivatives via Alkyne Hydroamination was written by Pan, Wan-Chen;Zhang, Mei-Mei;Liu, Jian-Quan;Wang, Xiang-Shan. And the article was included in Synthesis in 2019.Recommanded Product: 1186603-47-3 The following contents are mentioned in the article:

Using 2-(2-aminophenyl)quinazolin-4(3H)-one and 2-(2-phenylethynyl)benzaldehyde as the reactants, silver triflate (AgOTf) was proved to be an efficient catalyst to promote not only quinazoline cyclization, but also the intramol. hydroamination of alkyne for the synthesis of 6-aryl-17H,18aH-isoquinolino[2,1-a]quinazolino[3,2-c]quinazolin-17-one derivatives in high yields. This study involved multiple reactions and reactants, such as 5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3Recommanded Product: 1186603-47-3).

5-Chloro-2-(phenylethynyl)benzaldehyde (cas: 1186603-47-3) 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. 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: 1186603-47-3

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

Synthesis of substituted 1,3,5-triazines as tuberculostatic agents was written by Dave, M. P.;Patel, J. M.;Langalia, N. A.;Thaker, K. A.. And the article was included in Journal of the Indian Chemical Society in 1984.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:

A series of 2,4-bis(arylamino)-6-(pyridine-4-carboxhydrazido/substituted benzhydrazido)-1,3,5-triazines has been synthesized and tested against Mycobacterium tuberculosis strain H₂₇R_v. Some of them, e.g. I (R = o-, p-ClC₆H₄), have shown significant tuberculostatic 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. 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. 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

Preparation of some 2-(arylamino)-4-(4-carboxy-3-hydroxyanilino)-6-[α-(2-hydroxy-1-naphthyl)benzylamino]-s-triazine 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 1983.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:

Triaminotriazines I [R = Ph, substituted Ph, 1-naphthyl, CH₂Ph, R¹ = 3,4-HO(HO₂C)C₆H₃NH] were prepared by stepwise amination of cyanuric chloride. The products have bactericidal and tuberculostatic activity. Some intermediate I (R¹ = Cl) also have bactericidal activity. 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. 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.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine

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