13733-90-9

Basic information

• Product Name: 2,4-dichloro-6-(ethylsulfanyl)-1,3,5-triazine
• Synonyms: 2,4-DICHLORO-6-ETHYLTHIO-S-TRIAZINE
• CAS NO: 13733-90-9
• Molecular Formula: C₅H₅Cl₂N₃S
• Molecular Weight: 210.0843
• Mol File: 13733-90-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 395.3°C at 760 mmHg
• Flash Point: 192.9°C
• Density: 1.52g/cm³
• Vapor Pressure: 4.23E-06mmHg at 25°C
• Refractive Index: 1.598
• CAS DataBase Reference: 2,4-dichloro-6-(ethylsulfanyl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-6-(ethylsulfanyl)-1,3,5-triazine(13733-90-9)
• EPA Substance Registry System: 2,4-dichloro-6-(ethylsulfanyl)-1,3,5-triazine(13733-90-9)

Safety Data

• Hazardous Substances Data: 13733-90-9(Hazardous Substances Data)

Usage

Physical appearance

white to light yellow crystalline solid

Use

selective herbicide to control unwanted broadleaf and grassy weeds in various crops (e.g. corn, wheat, and rice)

Mechanism of action

inhibits the growth of weeds and disrupts their photosynthesis process

Mammalian toxicity

relatively low

Safety

considered safe for proper agricultural use when applied according to label instructions

Handling precautions

important to handle and use with care to avoid potential harm to humans, animals, and the environment.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 75-08-1 ethanethiol 

Relevant articles and documents

Triazine-Based Sequence-Defined Polymers with Side-Chain Diversity and Backbone-Backbone Interaction Motifs

Sequence control in polymers, well-known in nature, encodes structure and functionality. Here we introduce a new architecture, based on the nucleophilic aromatic substitution chemistry of cyanuric chloride, that creates a new class of sequence-defined polymers dubbed TZPs. Proof of concept is demonstrated with two synthesized hexamers, having neutral and ionizable side chains. Molecular dynamics simulations show backbone-backbone interactions, including H-bonding motifs and pi-pi interactions. This architecture is arguably biomimetic while differing from sequence-defined polymers having peptide bonds. The synthetic methodology supports the structural diversity of side chains known in peptides, as well as backbone-backbone hydrogen-bonding motifs, and will thus enable new macromolecules and materials with useful functions.