Phosphonic acid, propyl-, bis(1-methylethyl) ester

Base Information

Chemical Name:Phosphonic acid, propyl-, bis(1-methylethyl) ester
CAS No.:18812-55-0
Molecular Formula:C9H21O3P
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID50342321
Nikkaji Number:J2.057.466F
Wikidata:Q82113036

Synonyms:18812-55-0;Phosphonic acid, P-propyl-, bis(1-methylethyl) ester;Phosphonic acid, propyl-, bis(1-methylethyl) ester;Diisopropyl propylphosphonate #;SCHEMBL7739962;DTXSID50342321;Propylphosphonic acid diisopropyl ester;Phosphonic acid, propyl-, diisopropyl ester

Suppliers and Price of Phosphonic acid, propyl-, 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 4 raw suppliers

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

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:208.12283153
Heavy Atom Count:13
Complexity:164

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCP(=O)(OC(C)C)OC(C)C

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

There total 1 articles about Phosphonic acid, propyl-, 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: 1.0%

: 927-77-5
n-propylmagnesium bromide

: 132213-27-5
3-(diisopropoxyphosphinoyl)-5-phenylisoxazole

: 18812-55-0
diisopropyl n-propylphosphonate

: 1-phenyl-1-oxo-3-iminohexane

Guidance literature:: In diethyl ether; for 72h; Heating;
DOI:10.1007/BF01166315

Reference yield:

: 18812-55-0
diisopropyl n-propylphosphonate

: 1606168-19-7
isopropyl 5-{[6-(2-methoxyphenyl)pyrimidin-4-yl]amino}-2-methylphenyl propylphosphonate

Guidance literature:: Multi-step reaction with 2 steps

1.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 0 - 20 °C

2.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C

2.2: 20 °C

With oxalyl dichloride; potassium tert-butylate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm401742r

Reference yield:

: 18812-55-0
diisopropyl n-propylphosphonate

: 1606168-22-2
isopropyl 2-methyl-5-{[6-(3-nitrophenyl)pyrimidin-4-yl]amino}phenyl propylphosphonate

Guidance literature:: Multi-step reaction with 2 steps

1.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 0 - 20 °C

2.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 20 °C

2.2: 20 °C

With oxalyl dichloride; potassium tert-butylate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm401742r