949-42-8

Usage

Uses

Used in Marine Coatings Industry:
2,4-BIS(TRICHLOROMETHYL)-6-METHYL-1,3,5-TRIAZINE is used as an antifouling agent for marine coatings to prevent the growth of algae and other organisms on the hulls of ships and boats. This helps in reducing the drag caused by these organisms, improving the fuel efficiency and performance of the vessels.
However, due to the potential environmental and health hazards associated with its use, the application of 2,4-BIS(TRICHLOROMETHYL)-6-METHYL-1,3,5-TRIAZINE has been regulated and controlled in several countries. Exposure to this chemical has been linked to adverse effects on aquatic organisms and the environment, leading to concerns about its impact on marine ecosystems. As a result, alternative eco-friendly antifouling agents are being developed and promoted to minimize the potential harm to the environment.

InChI:InChI=1/C6H3Cl6N3/c1-2-13-3(5(7,8)9)15-4(14-2)6(10,11)12/h1H3

Upstream product

• 545-06-2 trichloroacetonitrile 
• 75-05-8 acetonitrile 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 542-02-9 2-methyl-4,6-diamino-1,3,5-triazine 
• 16352-06-0 6-methyl-5-azacytosine 
• 21227-47-4 4-methyl-6-trichloromethyl-[1,3,5]triazin-2-ylamine 
• 83256-21-7 2,4-bis(trichloromethyl)-6-(β-dimethylaminovinyl)triazine 
• 87019-98-5 2,4,6-tris[(E)-2-phenylethenyl]-1,3,5-triazine 
• 42573-57-9 2-(4-methoxystyryl)-4,6-bis(trichloromethyl)-1,3,5-triazine 
• 4000-78-6 2,4-Dimethoxy-6-methyl-1,3,5-triazin 

Relevant academic research and scientific papers

Preparation method of N-methyl triazine

The invention discloses a preparation method of N-methyl triazine. The preparation method comprises eight operation processes including BTCT preparation, low-temperature reaction, reflux reaction, salt filtering, distillation, amination, filtering and drying. Compared with the conventional preparation method, the preparation method provided by the invention has the obvious advantages in the aspects of lowering the safety risk, improving the product quality, reducing the work intensity, reducing the environment harm and the like.

POLYMERIZABLE COMPOUND, POLYMERIZABLE COMPOSITION, POLYMER, AND OPTICALLY ANISOTROPIC BODY

The present invention provides a polymerizable compound represented by the following formula (I), a polymerizable composition that includes the polymerizable compound and an initiator, a polymer obtained by polymerizing the polymerizable compound or the polymerizable composition, and an optically anisotropic article that includes the polymer. The invention makes it possible to provide a polymerizable compound, a polymerizable composition, and a polymer that have a practical low melting point, exhibit an excellent solubility in a general-purpose solvent, can be produced at low cost, and may produce an optical film that achieves uniform conversion of polarized light over a wide wavelength band, and an optically anisotropic article. [In formula: Q1 to Q4 represent hydrogen atoms or the like; X represents a C6-C12 divalent aromatic group or the like; Ax and Ay represent groups represented by the following formula (II); n represents 0 or 1; * represents a bonding position; Y1 to Y6 represent a single bond, -O-, -O-C(=O)-, -C(=O)-O- or the like; G1 and G2 represent divalent C1-C20 aliphatic groups or the like; Z1 and Z2 represent C2-C10 alkenyl groups or the like; A1 represents a trivalent aromatic group or the like; and A2 and A3 represent divalent C6-C30 aromatic groups or the like.]

6-Dialkylaminobenzimidazole nonlinear optical dyes

(Chemical Equation Presented) A new 6-dialkylaminobenzimidazole nonlinear optical dye was synthesized in eight linear steps with an overall yield of 16%.

Use of triazine derivatives for protecting maize and sorghum plants

There are described triazine derivatives of the formula I STR1 wherein R1, R2 and R3 independently of one another are each C1 -C5 -alkyl which is unsubstituted or monosubstituted by C3 -C6 -cycloalkyl, or mono- or polysubstituted by halogen, or is C3 -C6 - cycloalkyl which is unsubstituted or mono- or polysubstituted by halogen, or one of the substituents R1, R2 and R3 is also halogen or --NR4 R5, in which R4 is hydrogen or C1 -C5 -alkyl and R5 is hydrogen, C1 -C5 -alkyl, monochloroacetyl or dichloroacetyl. The triazine derivatives are used for the protection of maize and sorghum plants against the harmful effects of herbicidal chloroacetanilides and chloroacetamides.