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
• Article Data: 4

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

General Description

2-Butoxy-4,6-dichloro-1,3,5-triazine is a chemical compound used primarily as a herbicide. It belongs to the class of triazine herbicides, designed to kill unwanted plants by inhibiting photosynthesis. This chemical is known for its broad-spectrum weed control and is commonly used in agriculture and horticulture. However, it is important to handle this chemical with caution as it can be harmful if ingested or if it comes into contact with the skin or eyes. Proper safety measures and precautions should be taken when handling and using 2-butoxy-4,6-dichloro-1,3,5-triazine to avoid any adverse health effects.

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

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

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.

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.