Production Method 1

877-89-4

Reaction Conditions

Reference

Heterocyclic compounds. II. Syntheses of 1,3,5-triazine derivatives and their pharmacological activities. 2

Tsujikawa, Teruaki; Tsukamura, Kazuo; Takei, Saburo; Sirakawa, Kenzo; Chiba, Sukehiro; et al, Yakugaku Zasshi, 1975, 95(5), 521-20

Production Method 2

877-89-4

Reaction Conditions

1.1 Reagents: Sodium bicarbonate Solvents: Methanol ;  2 h, rt; rt → 50 °C; 22 h, 50 °C

Reference

Study of the Reactivities of Acid-Catalyzed O-Benzylating Reagents Based on Structural Isomers of 1,3,5-Triazine

Fujita, Hikaru; Hayakawa, Naoko; Kunishima, Munetaka, Journal of Organic Chemistry, 2015, 80(21), 11200-11205

Production Method 3

13320-09-7

877-89-4

Reaction Conditions

1.1 Solvents: Toluene
1.2 Solvents: Diethyl ether

Reference

1,3,5-Triazine-2,4,6-trisulfenyl trichloride. Synthesis, properties, and reactions

Tripolt, Robert; Schmuck, Siegfried; Nachbaur, Edgar, Zeitschrift fuer Naturforschung, 1999, 54(5), 609-616

Production Method 4

877-89-4

Reaction Conditions

1.1 Reagents: Sodium hydroxide Solvents: Methanol ;  30 °C; 2 h, rt

Reference

Synthesis and thermal decomposition of ditetrazol-5-ylamine

Nedel'ko, V. V.; Shastin, A. V.; Korsunskii, B. L.; Chukanov, N. V.; Larikova, T. S.; et al, Russian Chemical Bulletin, 2005, 54(7), 1710-1714

Production Method 5

27257-90-5

877-89-4

Reaction Conditions

1.1 Catalysts: Zinc nitrate Solvents: Methanol ;  3 h, 80 °C

Reference

Anion-Induced Assembly of Five-Coordinated Mercury(II) Complexes and Density Functional Theory Calculations to Study Bond Dissociation Energies of Long Hg-N Bonds

Zhou, Hong-Ping; Gan, Xiao-Ping; Li, Xian-Lei; Liu, Zhao-Di; Geng, Wen-Qian; et al, Crystal Growth & Design, 2010, 10(4), 1767-1776

Production Method 6

144-55-8

3140-73-6

877-89-4

Reaction Conditions

1.1 Solvents: Methanol

Reference

An improved procedure for the large scale preparation of 2-chloro-4,6-dimethoxy-1,3,5-triazine

Cronin, Jason S.; Ginah, Francis O.; Murray, Angela R.; Copp, James D., Synthetic Communications, 1996, 26(18), 3491-3494

Production Method 7

877-89-4

Reaction Conditions

Reference

Cyanuric acid derivatives. III. Alkoxy-s-triazines

Dudley, James R.; Thurston, Jack T.; Schaefer, Frederic C.; Holm-Hansen, Dagfrid; Hull, Clarence J.; et al, Journal of the American Chemical Society, 1951, 73, 2986-90

Production Method 8

877-89-4

Reaction Conditions

1.1 Reagents: 2-Pyridone Solvents: Methanol ;  4 h, 5 °C

Reference

A uniquely fabricated Cu(II)-metallacycle as a reusable highly sensitive dual-channel and practically functional metalloreceptor for Fe3+ and Ca2+ ions: an inorganic site of cation detection

Thakur, Neha; Pandey, Mrituanjay D.; Pandey, Rampal, New Journal of Chemistry, 2018, 42(5), 3582-3592

Production Method 9

3140-73-6

877-89-4

Reaction Conditions

Reference

Syntheses and reactions of cyano-1,3,5-triazines

Mori, Yasutomo; Kawakami, Satoshi; Hashida, Yoji, Nippon Kagaku Kaishi, 1990, (4), 396-400

Production Method 10

36335-90-7

877-89-4

Reaction Conditions

1.1 Reagents: Sodium methoxide

Reference

Regioselective reactions in heteroaromatic systems. Rules for methyl migration and nucleophilic substitution in methyl cyanurates and thiocyanurates

Tosato, Maria Livia; Soccorsi, Laura, Journal of the Chemical Society, 1982, (11), 1321-6

Production Method 11

63910-62-3

877-89-4

Reaction Conditions

Reference

Perhydrolysis of 2-chloro-4,6-dimethoxy-2-triazine

Speakman, Peter R. H., Chemistry & Industry (London, 1977, (6),

2,4,6-Trimethoxy-1,3,5-triazine Raw materials

• Sodium bicarbonate
• TPT
• [4,6-bis(chlorosulfanyl)-1,3,5-triazin-2-yl] Thiohypochlorite
• Chlorodimethoxytriazine
• 2,4-Dimethoxy-6-(methylthio)-1,3,5-triazine
• 1,3,5-Triazine, 2,2'-dioxybis[4,6-dimethoxy-

2,4,6-Trimethoxy-1,3,5-triazine Preparation Products

• 2,4,6-Trimethoxy-1,3,5-triazine (877-89-4)

• 1. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
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  Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Triazines 1,3,5-triazines Alkoxy-S-triazines

• 17635-40-4(2-methoxy-1,3,5-triazine)
• 108-80-5(Cyanuric acid)
• 24763-74-4(1,3,5-Triazine, 2,4,6-tris(ethenyloxy)-)
• 2250248-69-0(Methanimidic acid, 1,1',1''-(1,3,5-triazine-2,4,6-triyl) ester, sodium salt (1:3))
• 63910-63-4(1,3,5-Triazine, 2,2'-oxybis[4,6-dimethoxy-)
• 884-43-5(1,3,5-Triazine,2,4,6-triethoxy-)
• 1898-72-2(2,4-Dimethoxy-1,3,5-triazine)
• 72708-10-2(Poly(oxy-1,2-ethanediyl),a,a'-(6-chloro-1,3,5-triazine-2,4-diyl)bis[w-methoxy-)
• 63910-62-3(1,3,5-Triazine, 2,2'-dioxybis[4,6-dimethoxy-)
• 891-65-6(2-[[4,6-Bis(2-hydroxyethoxy)-1,3,5-triazin-2-yl]oxy]ethanol)