Phosphoramidic acid, (1-methylethyl)-, diethyl ester

Base Information

Chemical Name:Phosphoramidic acid, (1-methylethyl)-, diethyl ester
CAS No.:22685-19-4
Molecular Formula:C7H18 N O3 P
Molecular Weight:195.199
Hs Code.:
European Community (EC) Number:654-811-5
NSC Number:102505
UNII:UA9AFY82LV
DSSTox Substance ID:DTXSID50177216
Nikkaji Number:J500.396B
Wikidata:Q83047536
Mol file:22685-19-4.mol

Synonyms:Diethyl isopropylphosphoramidate;22685-19-4;Phosphoramidic acid, (1-methylethyl)-, diethyl ester;UA9AFY82LV;NSC-102505;N-diethoxyphosphorylpropan-2-amine;NSC102505;NSC 102505;UNII-UA9AFY82LV;SCHEMBL86162;DTXSID50177216;DIETHYL ISOPROPYLAMIDOPHOSPHATE;AKOS024332833;Diethoxy(isopropylamino)phosphine oxide;Diethyl N-(1-methylethyl)phosphoramidate;Phosphoramidic acid, isopropyl-, diethyl ester;Phosphoramidic acid, N-(1-methylethyl)-, diethyl ester

Suppliers and Price of Phosphoramidic acid, (1-methylethyl)-, diethyl 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 Phosphoramidic acid, (1-methylethyl)-, diethyl ester

Chemical Property:

Vapor Pressure:0.121mmHg at 25°C
Boiling Point:219.2°Cat760mmHg
Flash Point:86.4°C
Density:1.026g/cm³
XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:195.10243043
Heavy Atom Count:12
Complexity:151

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOP(=O)(NC(C)C)OCC

Technology Process of Phosphoramidic acid, (1-methylethyl)-, diethyl ester

There total 1 articles about Phosphoramidic acid, (1-methylethyl)-, diethyl 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: 91.0%

: 10220-34-5
N-isopropyl-2-benzothiazolesulfenamide

Diethyl phosphonate: 762-04-9,123-22-8
Diethyl phosphonate

: 22685-19-4
diethyl N-isopropylphosphoramidate

: 149-30-4,118090-09-8
2-Mercaptobenzothiazole

Guidance literature:: DOI:10.1246/cl.1980.695

Reference yield:

: 22685-19-4
diethyl N-isopropylphosphoramidate

: 104-15-4
toluene-4-sulfonic acid

: 84461-21-2
isopropylammonium tosylate

Guidance literature:: In ethanol; for 8h; Yield given; Heating;

Reference yield:

: 22685-19-4
diethyl N-isopropylphosphoramidate

: 29262-57-5
N-isopropyloxamic acid

Guidance literature:: Multi-step reaction with 3 steps

1: (COCl)2 / CCl₄ / Heating

2: diethyl ether

3: H₂O / Heating

With oxalyl dichloride; water; In tetrachloromethane; diethyl ether;