Dialifor

Base Information

• Chemical Name: Dialifor
• CAS No.: 10311-84-9
• Molecular Formula: C14H17 Cl N O4 P S2
• Molecular Weight: 393.852
• Hs Code.: 2933990011
• European Community (EC) Number: 233-689-3
• UN Number: 2811,2783
• UNII: 8480K0VB4E
• DSSTox Substance ID: DTXSID0037522
• Nikkaji Number: J3.118F
• Wikipedia: Dialifor
• Wikidata: Q5270555
• ChEMBL ID: CHEMBL1901826
• Mol file: 10311-84-9.mol

Synonyms:dialifor;O,O-diethyl S-(2-chloro-1-phthalimidoethyl) phosphorodithioate;Torak;Torak EC 24

Chemical Property of Dialifor

Chemical Property:

• Appearance/Colour: clear colorless liquid
• Vapor Pressure: 7.38E-09mmHg at 25°C
• Melting Point: 67-69oC
• Boiling Point: 465.9°Cat760mmHg
• PKA: -2.72±0.20(Predicted)
• Flash Point: 100℃
• PSA: 123.04000
• Density: 1.435g/cm³
• LogP: 4.46670
• Storage Temp.: 0-6°C
• Water Solubility.: 0.18mg/L(temperature not stated)
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 393.0025151
• Heavy Atom Count: 23
• Complexity: 473
• Transport DOT Label: Poison

Purity/Quality:

Dialifos ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Toxic by ingestion, cholinesterase inhibitor.
• Hazard Codes: T+,N
• Statements: 24-28-50/53
• Safety Statements: 28-36/37-45-60-61

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Pesticides -> Organophosphate Insecticides
• Canonical SMILES: CCOP(=S)(OCC)SC(CCl)N1C(=O)C2=CC=CC=C2C1=O
• Uses: Insecticide; acaricide. Nonsystemic insecticide and acaricide to control chewing and sucking insects and spider mites on a wide variety of fruits and vegetables.

Technology Process of Dialifor

There total 1 articles about Dialifor 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,O-diethyl S-(2-chloro-1-phthalimidoethyl)phosphorodithioate (10311-84-9)

Guidance literature:

Dichlorethylphthalimid, (EtO)2P(S)S^-NH4⁺;

Refernces

• 1、 -. "Condensation products". . . Retrieved 2008/06/13.