6625-15-6

Basic information

• Product Name: (2,4-dichlorophenyl)-diethoxyphosphoryl-methanol
• Synonyms: (2,4-dichlorophenyl)-diethoxyphosphoryl-methanol
• CAS NO: 6625-15-6
• Molecular Formula: C₁₁H₁₅Cl₂O₄P
• Molecular Weight: 313.11
• Mol File: 6625-15-6.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 614.5°C at 760 mmHg
• Flash Point: 325.5°C
• Appearance: /
• Density: 1.41g/cm³
• Vapor Pressure: 4.9E-15mmHg at 25°C
• Refractive Index: 1.67
• PKA: 11.43±0.20(Predicted)
• CAS DataBase Reference: (2,4-dichlorophenyl)-diethoxyphosphoryl-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4-dichlorophenyl)-diethoxyphosphoryl-methanol(6625-15-6)
• EPA Substance Registry System: (2,4-dichlorophenyl)-diethoxyphosphoryl-methanol(6625-15-6)

Safety Data

• Hazardous Substances Data: 6625-15-6(Hazardous Substances Data)

Usage

Description

(2,4-dichlorophenyl)-diethoxyphosphoryl-methanol, commonly known as Dicamba, is a chemical compound that functions as an herbicide and plant growth regulator. It is characterized by its ability to disrupt the normal growth and development of plants, leading to deformation and eventual death.
Used in Agricultural Industry:
Dicamba is used as a herbicide for controlling broadleaf weeds in agricultural settings. It is effective in managing unwanted plant growth that can compete with crops for resources, thus ensuring healthier and more productive fields.
Used in Residential Applications:
In residential areas, Dicamba serves as a herbicide to manage and control unwanted broadleaf weeds, contributing to the maintenance of lawns, gardens, and other green spaces.
However, it is important to note that the use of Dicamba has been surrounded by controversy due to its potential to drift and cause damage to nearby crops and vegetation. Additionally, there are concerns regarding its potential impact on human health and the environment. Therefore, strict regulation and monitoring of Dicamba use are essential to ensure its safe and responsible application.

InChI:InChI=1/C14H14N2O3S/c1-2-19-14-15-12(17)8-13(18)16(14)11(9-20-14)10-6-4-3-5-7-10/h3-7,9H,2,8H2,1H3,(H,15,17)

Upstream product

• 874-42-0 2,4-dichlorobenzaldeyhde 
• 122-52-1 triethyl phosphite 
• 762-04-9 phosphonic acid diethyl ester 

Downstream Products

• 1322881-52-6 diethyl [(3-chloro-4-methylanilinocarbonyl)oxy](2,4-dichlorophenyl)methyl phosphonate 
• 1146599-16-7 O,O-diethyl 1-[(6-chloropyridin-3-yl)methyl]-5-methyl-1H-1,2,3-triazol-4-ylcarbonyloxy-(2,4-dichlorophenyl)methyl-phosphonate 
• 153733-60-9 ((2,4-dichlorophenyl)(hydroxy)methyl)phosphonic acid 
• 1000281-17-3 chloro-acetic acid (2,4-dichloro-phenyl)-(diethoxy-phosphoryl)-methyl ester 

Relevant articles and documents

Isoprenoid Biosynthesis Inhibitors Targeting Bacterial Cell Growth

We synthesized potential inhibitors of farnesyl diphosphate synthase (FPPS), undecaprenyl diphosphate synthase (UPPS), or undecaprenyl diphosphate phosphatase (UPPP), and tested them in bacterial cell growth and enzyme inhibition assays. The most active compounds were found to be bisphosphonates with electron-withdrawing aryl-alkyl side chains which inhibited the growth of Gram-negative bacteria (Acinetobacter baumannii, Klebsiella pneumoniae, Escherichia coli, and Pseudomonas aeruginosa) at ～1–4 μg mL?1levels. They were found to be potent inhibitors of FPPS; cell growth was partially “rescued” by the addition of farnesol or overexpression of FPPS, and there was synergistic activity with known isoprenoid biosynthesis pathway inhibitors. Lipophilic hydroxyalkyl phosphonic acids inhibited UPPS and UPPP at micromolar levels; they were active (～2–6 μg mL?1) against Gram-positive but not Gram-negative organisms, and again exhibited synergistic activity with cell wall biosynthesis inhibitors, but only indifferent effects with other inhibitors. The results are of interest because they describe novel inhibitors of FPPS, UPPS, and UPPP with cell growth inhibitory activities as low as ～1–2 μg mL?1.

Synthesis, structure, and catalytic activity of novel trinuclear rare-earth metal amido complexes incorporating μ-η5:η1 bonding indolyl and μ3-oxo groups

The reactions of different pyrrolyl-functionalized indoles with rare-earth metal(iii) amides [(Me3Si)2N]3RE III(μ-Cl)Li(THF)3 (RE = Yb, Er, Dy, Eu, Y) produced different kinds of rare-earth metal amid

Rare-earth metal amido complexes supported by bridged bis(β- diketiminato) ligand as efficient catalysts for hydrophosphonylation of aldehydes and ketones

A series of rare-earth metal amides supported by a cyclohexyl-linked bis(β-diketiminato) ligand were synthesized, and their catalytic activities for hydrophosphonylation of aldehydes and ketones were developed. Reaction of [(Me3Si)2N