30894-93-0

Basic information

• Product Name: 2-chloro-4-(4-chlorophenyl)-6-phenyl-1,3,5-triazine
• Synonyms: 2-CHLORO-4-(P-CHLOROPHENYL)-6-PHENYL-S-TRIAZINE
• CAS NO: 30894-93-0
• Molecular Formula: C₁₅H₉Cl₂N₃
• Molecular Weight: 302.1581
• Mol File: 30894-93-0.mol

Chemical Properties

• Boiling Point: 505.7°C at 760 mmHg
• Flash Point: 291.2°C
• Density: 1.351g/cm³
• Vapor Pressure: 7.47E-10mmHg at 25°C
• Refractive Index: 1.629
• PKA: -0.62±0.10(Predicted)
• CAS DataBase Reference: 2-chloro-4-(4-chlorophenyl)-6-phenyl-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-4-(4-chlorophenyl)-6-phenyl-1,3,5-triazine(30894-93-0)
• EPA Substance Registry System: 2-chloro-4-(4-chlorophenyl)-6-phenyl-1,3,5-triazine(30894-93-0)

Safety Data

• Hazardous Substances Data: 30894-93-0(Hazardous Substances Data)

Usage

Uses

Used in Agriculture:
Chlortoluron is used as a pre-emergent herbicide for controlling annual grasses and broadleaf weeds in various crops such as apples, pears, plums, and cherries. It is applied to the soil before the weeds emerge, effectively preventing their growth and ensuring a healthy crop yield.
Used in Environmental Management:
Although chlortoluron has been banned in some countries due to its potential environmental and health risks, it was initially used to manage weed populations in agricultural settings. Its application helped maintain the quality of the soil and reduce the need for manual weed removal, thus contributing to more efficient and sustainable agricultural practices.

Upstream product

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Relevant articles and documents

Novel hetero-cyclic compound and organic light emitting device comprising the same

The present invention refers to novel heterocyclic compounds and organic light emitting device using the same number [...] substrate. (by machine translation)

Novel hetero-cyclic compound and organic light emitting device comprising the same

The present invention relates to a novel heterocyclic compound capable of increasing efficiency, low driving voltage and/or lifetime characteristics in an organic light emitting device, and an organic light emitting device using the same. The novel heterocyclic compound is represented by chemical formula 1. In chemical formula 1, L is phenylene, biphenylylene, or naphthylene, and Xs are each independently N or CH, wherein at least one of Xs is N.COPYRIGHT KIPO 2019

Novel hetero-cyclic compound and organic light emitting device comprising the same

The present invention relates to a novel heterocyclic compound capable of enhancing efficiency, and low driving voltage and/or lifespan characteristics in an organic light emitting device, and to an organic light emitting device using the same. The novel heterocyclic compound is represented by chemical formula 1. In chemical formula 1, Xs are each independently N or CH, wherein at least one of Xs is N, L_1 is a bond or substituted or unsubstituted C_(6-60) arylene.COPYRIGHT KIPO 2019

A Sequential Suzuki Coupling Approach to Unsymmetrical Aryl s-Triazines from Cyanuric Chloride

A practical approach has been developed for efficient synthesis of unsymmetrical aryl s-triazines via highly selective sequential Suzuki coupling of cyanuric chloride (2,4,6-trichlorotriazine) with aryl or vinyl boronic or diarylborinic acids catalysed by 0.1–0.5 mol% Pd(PPh3)2Cl2 under mild conditions. The second and third Suzuki couplings for unsymmetrically trisubstituted aryl s-triazines could be more practically conducted in one-pot procedure. An electron-withdrawing conjugate group at phenyl ring of arylboronic acids was unexpectedly found to completely block the coupling while steric hindrance from an ortho electron-donating substituent could be overcome. (Figure presented.).