Phenidet

Base Information

• Chemical Name: Phenidet
• CAS No.: 6784-53-8
• Molecular Formula: C10H14N3OP
• Molecular Weight: 223.2114
• NSC Number: 514541
• UNII: V8K89YHR6G
• DSSTox Substance ID: DTXSID00218082
• Nikkaji Number: J1.397.994D
• Wikidata: Q83094835
• Mol file: 6784-53-8.mol

Synonyms:Phenidet;Bis(1-ethylenimino)phosphoxyanilide;Phosphine oxide, anilinobis(1-aziridinyl)-;Phosphinic amide, P,P-bis(1-aziridinyl)-N-phenyl-;NSC 514541;Phosphine oxide, bis(1-aziridinyl)(phenylamino)-;6784-53-8;AI3-62258;Phosphoramide, N,N'-diethylene-N''-phenyl-;Aziridine, 1,1'-(anilinophosphinylidene)bis-;P,P-Bis(1-aziridinyl)-N-phenylphosphinic amide;Phosphoric triamide, N,N'-diethylene-N''-phenyl-;BRN 0190775;V8K89YHR6G;NSC-514541;4-20-00-00046 (Beilstein Handbook Reference);UNII-V8K89YHR6G;C10H14N3OP;SCHEMBL6936801;DTXSID00218082;C10-H14-N3-O-P;NSC514541;N-Phenylbis(1-aziridinyl)phosphinamide;Anilinobis(1-aziridinyl)phosphine oxide;Phosphoramide,N'-diethylene-N''-phenyl-;Aziridine,1'-(anilinophosphinylidene)bis-;LS-106253;Phosphoric triamide,N'-diethylene-N''-phenyl-;Phosphinic amide,P-bis(1-aziridinyl)-N-phenyl-;P,P-Di(1-aziridinyl)-N-phenylphosphinic amide #

Chemical Property of Phenidet

Chemical Property:

• Vapor Pressure: 9.83E-05mmHg at 25°C
• Boiling Point: 338.4°Cat760mmHg
• Flash Point: 158.5°C
• Density: 1.35g/cm³
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 223.08744908
• Heavy Atom Count: 15
• Complexity: 266

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CN1P(=O)(NC2=CC=CC=C2)N3CC3

Technology Process of Phenidet

There total 2 articles about Phenidet 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:

ethyleneimine (151-56-4,9002-98-6) + phenylamidophosphoric dichloride (6955-57-3) → N-Phenyl-N',N''-diethylenetriamide of phosphoric acid (6784-53-8)

Guidance literature:

With triethylamine; benzene;

Reference yield:

→ N-Phenyl-N',N''-diethylenetriamide of phosphoric acid (6784-53-8)

Guidance literature:

Phosphorsaeure-anilid-dichlorid, Aethylenimin, Bzl.;

Reference yield: 89.0%

N-Phenyl-N',N''-diethylenetriamide of phosphoric acid (6784-53-8) → N-Phenyl-N',N''-bis(S-dilithiophosphoryl-β-mercaptoethyl)triamidophosphate (83822-72-4)

Guidance literature:

With hydrogenchloride; lithium thiophosphate powder; In water; for 0.333333h; Ambient temperature;

DOI:10.1007/BF00513431

upstream raw materials:

ethyleneimine

phenylamidophosphoric dichloride

Downstream raw materials:

N-Phenyl-N',N''-bis(S-dilithiophosphoryl-β-mercaptoethyl)triamidophosphate