Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) ester

Base Information

Chemical Name:Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) ester
CAS No.:141543-26-2
Molecular Formula:C13H18FO4P
Molecular Weight:288.256
Hs Code.:
DSSTox Substance ID:DTXSID90403687

Synonyms:141543-26-2;Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) ester;DTXSID90403687

Suppliers and Price of Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) ester

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:288.09267421
Heavy Atom Count:19
Complexity:343

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)OP(=O)(C(=O)C1=CC=CC=C1F)OC(C)C

Technology Process of Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) ester

There total 1 articles about Phosphonic acid, (2-fluorobenzoyl)-, bis(1-methylethyl) 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: 86.0%

: 116-17-6
triisopropyl phosphite

: 393-52-2
2-Fluorobenzoyl chloride

: 141543-26-2
Diisopropyl 2-fluorobenzoylphosphonate

Guidance literature:: at 80 ℃; for 2h;

Reference yield:

: 141543-26-2
Diisopropyl 2-fluorobenzoylphosphonate

: (S)-Diisopropyl (2-fluorophenyl)hydroxymethylphosphonate

: (R)-Diisopropyl (2-fluorophenyl)hydroxymethylphosphonate

Guidance literature:: With (S)-tetrahydro-1-butyl-3,3-diphenyl-1H,3H-pyrrolo{2,1-c}{1,3,2}oxazaborole; benzo[1,3,2]dioxaborole; In tetrahydrofuran; toluene; at -20 ℃; for 5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1016/0957-4166(95)00132-9