Agn-PC-006iws

Base Information

• Chemical Name: Agn-PC-006iws
• CAS No.: 22289-00-5
• Molecular Formula: C₁₀H₂₃O₃P
• Molecular Weight: 222.265
• DSSTox Substance ID: DTXSID50461960
• Wikidata: Q82286420
• Mol file: 22289-00-5.mol

Synonyms:AGN-PC-006IWS;22289-00-5;SCHEMBL672872;DTXSID50461960

Chemical Property of Agn-PC-006iws

Chemical Property:

• XLogP3: 3.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 221.13065656
• Heavy Atom Count: 14
• Complexity: 169

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)CO[P+](=O)OCC(C)(C)C

Technology Process of Agn-PC-006iws

There total 1 articles about Agn-PC-006iws 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:

2,2-dimethyl-propanol-1 (75-84-3) + 2,4,6-tris(2,6-di-tert-butyl-4-methylphenoxy)-1,3,5,2,4,6,trioxatriphosphorinane (96357-74-3) → Dineopentyl H-phosphonate (22289-00-5) + C20H35O3P

Guidance literature:

Multistep reaction. Title compound not separated from byproducts; 1.) 300-350 deg C, 1E-6 to 1E-5 torr, 2.) -195 deg C to r.t.;

DOI:10.1021/jo00121a042

Reference yield:

Dineopentyl H-phosphonate (22289-00-5) → C23H45N2O3PSe (81017-65-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 68 percent / triethylamin, selenium / benzene / 72 h / Ambient temperature

2: diethyl ether / Ambient temperature

With selenium; triethylamine; In diethyl ether; benzene;

DOI:10.1021/jo00179a028

Reference yield:

Dineopentyl H-phosphonate (22289-00-5) → C25H37N2O3PSe (64674-21-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 68 percent / triethylamin, selenium / benzene / 72 h / Ambient temperature

2: diethyl ether / Ambient temperature

With selenium; triethylamine; In diethyl ether; benzene;

DOI:10.1021/jo00179a028

upstream raw materials:

2,2-dimethyl-propanol-1

2,4,6-tris(2,6-di-tert-butyl-4-methylphenoxy)-1,3,5,2,4,6,trioxatriphosphorinane

Downstream raw materials:

C₂₃H₄₅N₂O₃PSe

C₂₅H₃₇N₂O₃PSe

C₂₃H₃₁Cl₂N₂O₃PSe