Edifenphos

Base Information

• Chemical Name: Edifenphos
• CAS No.: 17109-49-8
• Molecular Formula: C14H15O2PS2
• Molecular Weight: 310.378
• Hs Code.: 2930909058
• European Community (EC) Number: 241-178-1
• UNII: 770M9U0F8Q
• DSSTox Substance ID: DTXSID7041910
• Nikkaji Number: J3.449E
• Wikipedia: Edifenphos
• Wikidata: Q15632710
• Metabolomics Workbench ID: 45094
• ChEMBL ID: CHEMBL1671900
• Mol file: 17109-49-8.mol

Synonyms:Bay 78418;edifenphos;Hinosan;O-ethyl-S,S-diphenyl phosphorodithioate

Chemical Property of Edifenphos

Chemical Property:

• Appearance/Colour: Yellow to brown liquid with a characteristic odor.
• Vapor Pressure: 3.32E-07mmHg at 25°C
• Melting Point: 25°C
• Refractive Index: 1.618
• Boiling Point: 430.2 °C at 760 mmHg
• Flash Point: 214 °C
• PSA: 86.71000
• Density: 1.27 g/cm³
• LogP: 5.71560
• Storage Temp.: 0-6°C
• Water Solubility.: 56 mg l-1 (20 °C)
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 310.02510906
• Heavy Atom Count: 19
• Complexity: 276

Purity/Quality:

98+% ^*data from raw suppliers

EDDP ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T, N
• Hazard Codes: T,N
• Statements: 21-23/25-43-50/53-24/25-23
• Safety Statements: 36/37-45-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Fungicides
• Canonical SMILES: CCOP(=O)(SC1=CC=CC=C1)SC2=CC=CC=C2
• Uses: Fungicide. Edifenphos is a foliar applied contact fungicide that provides both protective and curative control of rice blast diseases caused by Pyricularia oryzae. It also controls ear blight and stem rot in rice.

Technology Process of Edifenphos

There total 1 articles about Edifenphos 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:

→ O-ethyl diphenyl phosphorodithioate (17109-49-8)

Guidance literature:

Refernces

• 1、 -. "Synergistic Active Compound Combinations Comprising Phenyltriazoles". . . Retrieved 2011/07/29.
• 2、 -. "Delta1-pyrrolines used as pesticides". . . Retrieved 2008/06/13.