Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester

Base Information

Chemical Name:Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester
CAS No.:106052-22-6
Molecular Formula:C13H21O4P
Molecular Weight:272.281
Hs Code.:
DSSTox Substance ID:DTXSID90544347
Nikkaji Number:J721.719F
Wikidata:Q82421445

Synonyms:106052-22-6;Dipropan-2-yl (4-methoxyphenyl)phosphonate;DTXSID90544347

Suppliers and Price of Phosphonic acid, (4-methoxyphenyl)-, 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
Packaging
price

Total 0 raw suppliers

Chemical Property of Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:272.11774614
Heavy Atom Count:18
Complexity:269

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Phosphonic acid, (4-methoxyphenyl)-, bis(1-methylethyl) ester

There total 16 articles about Phosphonic acid, (4-methoxyphenyl)-, 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: 99.0%

: 104-92-7
1-bromo-4-methoxy-benzene

: 1809-20-7
diisopropyl hydrogenphosphonate

: 106052-22-6
diisopropyl (p-methoxyphenyl)phosphonate

Guidance literature:: With C₃₇H₃₃ClFeNPPd⁽¹⁺⁾; potassium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 2h; Inert atmosphere;
DOI:10.1002/ejoc.201201230

Reference yield: 99.0%

: 1809-20-7
diisopropyl hydrogenphosphonate

: 623-12-1
4-chloromethoxybenzene

: 106052-22-6
diisopropyl (p-methoxyphenyl)phosphonate

Guidance literature:: With C₃₈H₃₆Cl₂Fe₂N₂Pd₂⁽²⁺⁾; potassium tert-butylate; XPhos; In N,N-dimethyl acetamide; at 130 ℃; for 3h; Reagent/catalyst; Inert atmosphere;
DOI:10.1002/ejoc.201201230

Reference yield: 96.0%

: 1809-20-7
diisopropyl hydrogenphosphonate

: 4-methoxyphenyl(trimethyl)ammonium tetrafluoroborate

: 106052-22-6
diisopropyl (p-methoxyphenyl)phosphonate

Guidance literature:: With bis(1,5-cyclooctadiene)nickel ⁽⁰⁾; potassium phosphate; 2-(di-tert-butylphosphaneyl)-4-methoxy-N,N-dimethylaniline; In tetrahydrofuran; acetonitrile; at 80 ℃; for 5h; Schlenk technique; Inert atmosphere;
DOI:10.1134/S1070428021060117