Phosacetim

Base Information

• Chemical Name: Phosacetim
• CAS No.: 4104-14-7
• Deprecated CAS: 4157-35-1
• Molecular Formula: C14H13Cl2N2O2PS
• Molecular Weight: 375.215
• Hs Code.: 2931900090
• European Community (EC) Number: 223-874-7
• UN Number: 2783
• UNII: 7B08Z34L7O
• DSSTox Substance ID: DTXSID5040330
• Wikipedia: Phosacetim
• Mol file: 4104-14-7.mol

Synonyms:Gophacide;phosacetim

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Chemical Property of Phosacetim

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 104-106oC
• Boiling Point: 477.242°C at 760 mmHg
• PKA: 2.67±0.50(Predicted)
• Flash Point: 242.427°C
• PSA: 96.24000
• Density: 1.43g/cm³
• LogP: 6.40370
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 373.9812412
• Heavy Atom Count: 22
• Complexity: 409

Purity/Quality:

Safty Information:

• Pictogram(s): T+,N
• Hazard Codes: T+,N
• Statements: 27/28-50/53
• Safety Statements: 28-36/37-45-60-61

MSDS Files:

Useful:

• Chemical Classes: Pesticides -> Rodenticides
• Canonical SMILES: CC(=NP(=S)(OC1=CC=C(C=C1)Cl)OC2=CC=C(C=C2)Cl)N
• Isomeric SMILES: C/C(=N\P(=S)(OC1=CC=C(C=C1)Cl)OC2=CC=C(C=C2)Cl)/N
• Description: Phosacetim is a white crystalline powder in appearance. It is a toxic organophosphate compound used as a rodenticide and acts as an inhibitor of acetylcholinesterase enzyme. On heating, phosacetim undergoes decomposition to emit toxic fumes, primarily chlorides and oxides of nitrogen, sulphur, and phosphorus. Phosacetim is susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidising agents may result in the release of toxic phosphorus oxides.

Technology Process of Phosacetim

There total 1 articles about Phosacetim 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:

→ gophacide (4104-14-7)

Guidance literature: