Phosphonic acid, (1-aminoethyl)-, diphenyl ester

Base Information

Chemical Name:Phosphonic acid, (1-aminoethyl)-, diphenyl ester
CAS No.:73270-41-4
Molecular Formula:C14H16NO3P
Molecular Weight:277.25600
Hs Code.:
DSSTox Substance ID:DTXSID20454405
Nikkaji Number:J1.739.460F

Synonyms:Phosphonic acid, (1-aminoethyl)-, diphenyl ester;73270-41-4;SCHEMBL7623135;diphenyl 1-aminoethanephosphonate;DTXSID20454405;1-Aminoethylphosphonic acid diphenyl ester

Suppliers and Price of Phosphonic acid, (1-aminoethyl)-, diphenyl ester

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Phosphonic acid, (1-aminoethyl)-, diphenyl ester

Chemical Property:

PSA：71.36000
LogP:4.34250
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:277.08678037
Heavy Atom Count:19
Complexity:288

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(N)P(=O)(OC1=CC=CC=C1)OC2=CC=CC=C2

Technology Process of Phosphonic acid, (1-aminoethyl)-, diphenyl ester

There total 2 articles about Phosphonic acid, (1-aminoethyl)-, diphenyl 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:

: 65164-80-9
diphenyl 1-(phenylmethoxycarbonylamino)ethyl phosphonate

: 73270-41-4
(L,D)-diphenyl 1-aminoethylphosphonate

Guidance literature:: With hydrogen bromide; acetic acid;
DOI:10.1055/s-1979-28903

Reference yield:

: 101-02-0
triphenyl phosphite

: 73270-41-4
(L,D)-diphenyl 1-aminoethylphosphonate

Guidance literature:: Multi-step reaction with 2 steps

1: glacial AcOH / a) 50 deg C, 2 h, b) RT, 2 h

2: 30 percent HBr, AcOH / 1.5 h / Ambient temperature

With hydrogen bromide; acetic acid;
DOI:10.1021/ja983017e