(E)-Tetrachlorvinphos

Base Information

• Chemical Name: (E)-Tetrachlorvinphos
• CAS No.: 961-11-5
• Molecular Formula: C10H9Cl4O4P
• Molecular Weight: 365.965
• Hs Code.: 29199000
• European Community (EC) Number: 213-506-3,244-865-4,630-735-8
• UN Number: 2783
• UNII: YK4U8Y15ME
• DSSTox Substance ID: DTXSID2058334
• Nikkaji Number: J87.300D
• Wikipedia: Tetrachlorvinphos
• Wikidata: Q2406710
• Mol file: 961-11-5.mol

Synonyms:Gardona;Rabon;Stirofos;Tetrachlorvinphos

Chemical Property of (E)-Tetrachlorvinphos

Chemical Property:

• Appearance/Colour: Colorless crystals or white powder
• Vapor Pressure: 3.14E-06mmHg at 25°C
• Melting Point: 94-97oC
• Refractive Index: 1.553
• Boiling Point: 399.5 °C at 760 mmHg
• Flash Point: 302.8 °C
• PSA: 54.57000
• Density: 1.52 g/cm³
• LogP: 5.60150
• Water Solubility.: 11mg/L(20 oC)
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 365.896306
• Heavy Atom Count: 19
• Complexity: 371

Purity/Quality:

99.9% ^*data from raw suppliers

TETRACHLORVINPHOS 98.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Organophosphate Insecticides
• Canonical SMILES: COP(=O)(OC)OC(=CCl)C1=CC(=C(C=C1Cl)Cl)Cl
• Isomeric SMILES: COP(=O)(OC)O/C(=C/Cl)/C1=CC(=C(C=C1Cl)Cl)Cl
• Description: Tetrachlorvinphos belongs to a kind of organophosphate) insecticide with low toxicity on mammals. It is mainly used for the treatment of fleas, ticks, many kinds of flies, lice and insect larvae emerging on livestock and pets as well as their premises. Its formulation includes dust, pet collars, emulsifiable concentrates, feed additives, feed blocks, wettable powders, pellets and granular products. It takes effect through inhibiting the activity of organophosphate cholinesterase of pests.

Technology Process of (E)-Tetrachlorvinphos

There total 1 articles about (E)-Tetrachlorvinphos which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Tetrachlorovinphos (961-11-5)

Guidance literature:

2,2,2',4',5'-Pentachloracetophenon (I), Trimethylphosphit, Δ;

Reference yield: 88.0%

Tetrachlorovinphos (961-11-5) → 2-Chlor-1-(2,4,5-trichlorphenyl)-vinyl-methylhydrogen-phosphat (14299-52-6)

Guidance literature:

With sodium bromide; N-benzyl-N,N,N-triethylammonium chloride; In acetonitrile; for 8h; Heating;

DOI:10.1055/s-1983-30374

Reference yield:

Tetrachlorovinphos (961-11-5) → C8H3Cl6O2P (52417-99-9)

Guidance literature:

With phosphorus pentachloride; trichlorophosphate;

Downstream raw materials:

C₈H₃Cl₆O₂P

2-Chlor-1-(2,4,5-trichlorphenyl)-vinyl-methylhydrogen-phosphat

Phosphoramidic acid (E)-2-chloro-1-(2,4,5-trichloro-phenyl)-vinyl ester methyl ester

Methyl-phosphoramidic acid (E)-2-chloro-1-(2,4,5-trichloro-phenyl)-vinyl ester methyl ester