Phosphoramidic acid, phenyl-, dipentyl ester

Base Information

• Chemical Name: Phosphoramidic acid, phenyl-, dipentyl ester
• CAS No.: 101725-00-2
• Molecular Formula: C₁₆H₂₈NO₃P
• Molecular Weight: 313.377
• DSSTox Substance ID: DTXSID10144146
• Wikidata: Q83008243
• Mol file: 101725-00-2.mol

Synonyms:Di-n-amyl anilidophosphate;Phenylphosphoramidic acid dipentyl ester;Phosphoramidic acid, phenyl-, dipentyl ester;BRN 3388747;101725-00-2;C16H28NO3P;DTXSID10144146;C16-H28-N-O3-P;LS-107357

Chemical Property of Phosphoramidic acid, phenyl-, dipentyl ester

Chemical Property:

• Vapor Pressure: 3.82E-06mmHg at 25°C
• Boiling Point: 385.4°Cat760mmHg
• Flash Point: 186.9°C
• Density: 1.064g/cm³
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 12
• Exact Mass: 313.18068075
• Heavy Atom Count: 21
• Complexity: 277

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCOP(=O)(NC1=CC=CC=C1)OCCCCC

Technology Process of Phosphoramidic acid, phenyl-, dipentyl ester

There total 4 articles about Phosphoramidic acid, phenyl-, dipentyl ester 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:

phosphonic acid dipentyl ester (1809-17-2) → phenyl-amidophosphoric acid dipentyl ester (101725-00-2)

Guidance literature:

Multi-step reaction with 2 steps

1: sulfuryl chloride

With sulfuryl dichloride;

DOI:10.1021/ja01103a535

Reference yield:

pentan-1-ol (71-41-0) → phenyl-amidophosphoric acid dipentyl ester (101725-00-2)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrachloromethane; phosphorus (III)-chloride

2: sulfuryl chloride

With tetrachloromethane; sulfuryl dichloride; phosphorus trichloride;

DOI:10.1021/ja01103a535

Reference yield:

di-n-pentyl phosphorchloridate (14254-40-1) + aniline (62-53-3) → phenyl-amidophosphoric acid dipentyl ester (101725-00-2)

Guidance literature:

DOI:10.1021/ja01103a535

upstream raw materials:

phosphonic acid dipentyl ester

aniline

di-n-pentyl phosphorchloridate

pentan-1-ol