13838-32-9

Basic information

• Product Name: 2-BUTOXY-4,6-DICHLORO-1,3,5-TRIAZINE
• Synonyms: 2-BUTOXY-4,6-DICHLORO-1,3,5-TRIAZINE;2-n-Butoxy-4,6-dichloro-1,3,5-triazine
• CAS NO: 13838-32-9
• Molecular Formula: C₇H₉Cl₂N₃O
• Molecular Weight: 222.07
• EINECS: 237-555-5
• Mol File: 13838-32-9.mol

Chemical Properties

• Boiling Point: 357.5°Cat760mmHg
• Flash Point: 170°C
• Appearance: /
• Density: 1.333g/cm³
• Vapor Pressure: 5.6E-05mmHg at 25°C
• Refractive Index: 1.523
• CAS DataBase Reference: 2-BUTOXY-4,6-DICHLORO-1,3,5-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BUTOXY-4,6-DICHLORO-1,3,5-TRIAZINE(13838-32-9)
• EPA Substance Registry System: 2-BUTOXY-4,6-DICHLORO-1,3,5-TRIAZINE(13838-32-9)

Safety Data

• Hazardous Substances Data: 13838-32-9(Hazardous Substances Data)

Usage

Uses

Used in Agricultural Applications:
2-Butoxy-4,6-dichloro-1,3,5-triazine is used as a herbicide for its ability to effectively control a wide range of unwanted plants. It is particularly valuable in agriculture for maintaining crop health by eliminating competing vegetation, thus ensuring optimal growth conditions and yield.
Used in Horticultural Applications:
In horticulture, 2-Butoxy-4,6-dichloro-1,3,5-triazine is utilized to manage weed growth around ornamental plants and in landscaping. Its broad-spectrum control helps maintain the aesthetic appeal of gardens and other cultivated areas by preventing the overgrowth of weeds that can detract from the desired visual impact.

InChI:InChI=1/C7H9Cl2N3O/c1-2-3-4-13-7-11-5(8)10-6(9)12-7/h2-4H2,1H3

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 71-36-3 butan-1-ol 

Downstream Products

• 1267551-03-0 C₄₂H₄₂Cl₃N₁₅O₃ 
• 1267551-02-9 2,4,6-tri(4-(4-butyloxy-6-chloro-1,3,5-triazin-2-yl)phenyl)-1,3,5-triazine 
• 1267551-14-3 1,3,5-tri(4-(4-butyloxy-6-chloro-1,3,5-triazin-2-yl)oxyphenyl)benzene 
• 92498-59-4 6-(4-phenylphenyl)-1,3,5-triazine-2,4-diol 

Relevant articles and documents

Triazine natural gas drag reducer as well as synthesis method and application thereof

The invention discloses a triazine natural gas drag reducer and a synthesis method thereof. The molecular structural formula of the drag reducer is shown in the description. The synthesis method of the drag reducer comprises the following steps: dissolving cyanuric chloride in a solvent, dropwise adding an alcohol and an inorganic alkali at -15-0 DEG C, carrying out a reaction at -15-0 DEG C for 2-6 h, adding morpholine and the inorganic alkali after the reaction ends, carrying out a reaction at 50-100 DEG C for 6-12 h, washing the obtained reaction product with water after the reaction ends,and drying the washed reaction product to obtain the product. The drag reducer has a multi-polar end and a non-polar end, and has a good adsorption performance and excellent drag reducing and transportation increasing effects. The synthesis method has the advantages of simplicity, mild conditions, short time, low device requirements, and easiness in realization of large-scale industrial production.

Design, Synthesis and Biological Evaluation of Novel Nonsteroidal Progesterone Receptor Antagonists Based on Phenylamino-1,3,5-triazine Scaffold

We report here the development of phenylamino-1,3,5-triazine derivatives as novel nonsteroidal progesterone receptor (PR) antagonists. PR plays key roles in various physiological systems, including the female reproductive system, and PR antagonists are promising candidates for clinical treatment of multiple diseases. By using the phenylamino-1,3,5-triazine scaffold as a template structure, we designed and synthesized a series of 4-cyanophenylamino-1,3,5-triazine derivatives. The synthesized compounds exhibited PR antagonistic activity, and among them, compound 12n was the most potent (IC50=0.30μM); it also showed significant binding affinity to the PR ligand-binding domain. Docking simulation supported the design rationale of the compounds. Our results suggest that the phenylamino-1,3,5-triazine scaffold is a versatile template for development of nonsteroidal PR antagonists and that the developed compounds are promising lead compounds for further structural development of nonsteroidal PR antagonists.

Synthesis and functionalization of heteroatom-bridged bicyclocalixaromatics, large molecular triangular prisms with electron-rich and -deficient aromatic interiors

The synthesis and functionalization of oxygen and nitrogen atom bridged bicyclocalixaromatics of triangular prism structures are reported. By means of a fragment coupling approach, molecular triangular prisms of electron-rich and electron-deficient aromatic interiors were prepared using 1,3,5-tri(p- hydroxyphenyl)benzene and 2,4,6-tri(p-aminophenyl) triazine as base units and chlorotriazines as pillars. Aromatic nucleophilic substitution reaction of chlorotriazine moieties with functionalized amines led to triangular prisms with functionalizations on the peripheral edge positions, while functionalized triangular prisms on the vertex nitrogen positions were obtained using 2,4,6-tri[(p-allylamino)phenyl]-triazine derivative as a starting material. Symmetrical and distorted molecular triangular prisms in the solid state were revealed by X-ray crystallography. As evidenced by NMR spectroscopic data, however, all cage molecules synthesizedmost probably adopted highly symmetric triangular prism structures in solution phase. The functionalized shape-persistent triangular prism structures might find applications in molecular recognition and in the construction of higher and more sophisticated molecular architectures in supramolecular chemistry.

IMPROVEMENT OF THE SELECTIVITY OF ALKOXYLATION OF CYANURIC CHLORIDE.

Study of the quantitative relationships of the alkoxylation reaction and optimization of the complex reaction based on a mathematical model show that individual monoalkoxy-s-triazines free from 5-15% of dialkoxy-s-triazines cannot be obtained in aqueous acetone solutions. It is found that if the reaction is conducted in the basic bipolar aprotic solvent dimethylacetamide it proceeds selectively with exclusive formation of monoalkoxy-s-triazines. It can be seen from the data that the nature of the solvent does not affect selectivity of the reaction significantly. It is shown that when cyanuric chloride reacts with amides left bracket dimethylformamide (DMFA), N-methylformamide right bracket hygroscopic hydrolytically unstable products of the salt type are formed. The intermediates react with nucleophiles, such as aniline, to form substituted triazines. The reaction proceeds analogously with alcohols, and the hydrogen chloride evolved is bound irreversibly by dimethylacetamide.