69640-38-6

Basic information

• Product Name: 2,4-dichloro-6-(3,4,5-trichloro-1H-pyrrol-2-yl)phenol
• CAS NO: 69640-38-6
• Molecular Formula: C₁₀H₄Cl₅NO
• Molecular Weight: 331.4099
• Mol File: 69640-38-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 445.9°C at 760 mmHg
• Flash Point: 223.5°C
• Density: 1.733g/cm³
• Vapor Pressure: 1.45E-08mmHg at 25°C
• Refractive Index: 1.672
• CAS DataBase Reference: 2,4-dichloro-6-(3,4,5-trichloro-1H-pyrrol-2-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-6-(3,4,5-trichloro-1H-pyrrol-2-yl)phenol(69640-38-6)
• EPA Substance Registry System: 2,4-dichloro-6-(3,4,5-trichloro-1H-pyrrol-2-yl)phenol(69640-38-6)

Safety Data

• Hazardous Substances Data: 69640-38-6(Hazardous Substances Data)

Usage

General Description

2,4-dichloro-6-(3,4,5-trichloro-1H-pyrrol-2-yl)phenol is a chemical compound with a complex molecular structure. It contains two chlorine atoms and a pyrrole ring, which is a five-membered aromatic heterocycle. 2,4-dichloro-6-(3,4,5-trichloro-1H-pyrrol-2-yl)phenol is a potent fungicide and is commonly used in agricultural applications to control fungal diseases in crops. It works by inhibiting the growth and reproduction of fungi, ultimately protecting plant health and crop yield. Due to its chemical properties, it is important to handle this compound with care and follow safety guidelines when using it in agricultural or industrial settings.

Upstream product

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• 69640-33-1 2-(3,5-dichloro-2-methoxyphenyl)-1H-pyrrole 
• 69640-34-2 2,3,4-trichloro-5-(3,5-dichloro-2-methoxyphenyl)-1H-pyrrole 

Relevant articles and documents

C–H Arylation of N-Heteroarenes under Metal-Free Conditions and its Application towards the Synthesis of Pentabromo- and Pentachloropseudilins

Herein, we are reporting metal-free conditions for radical initiation and direct C–H arylation of N-heteroarenes. Starting from aniline, the corresponding arenediazonium salt generated in situ is reduced to an aryl radical in the presence of chloropromazine hydrochloride, a new reagent for this application. The optimized procedures are mild, operationally simple, and are working successfully with more diverse substrates in comparison to reported methods. The optimized method is also employed for the synthesis of marine natural products Pentabromo- and Pentachloropseudilins (PBP/PCP). In the present study, we also validated the potential of the Pentachloropseudilin (PCP), thus synthesized, for inhibition of Myosin1 function in mammalian cells and confirmed that PCP phenocopies Myosin1c depletion in cells.

MEANS FOR TREATING MYOSIN-RELATED DISEASES

The present invention provides a method of designing a modulator of a myosin, the method comprising molecular modeling of a compound such that the modeled compound interacts with at least three amino acid residues of said myosin, said residues being selec