Aminoethylphosphinic acid

Base Information

Chemical Name:Aminoethylphosphinic acid
CAS No.:71937-28-5
Molecular Formula:C2H8 N O2 P
Molecular Weight:109.065
Hs Code.:
European Community (EC) Number:426-930-0
UNII:G4888SY0QO
DSSTox Substance ID:DTXSID50995871
Wikidata:Q27278734
ChEMBL ID:CHEMBL37702
Mol file:71937-28-5.mol

Synonyms:1-aminoethylphosphinate;1-aminoethylphosphinic acid;1-aminoethylphosphinic acid, (+)-isomer;1-aminoethylphosphinic acid, (+-)-isomer;1-aminoethylphosphinic acid, sodium salt, (+-)-isomer

Suppliers and Price of Aminoethylphosphinic acid

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 Aminoethylphosphinic acid

Chemical Property:

PSA：95.92000
LogP:-0.25280
XLogP3:-1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:108.02144046
Heavy Atom Count:6
Complexity:64.6

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(N)[P+](=O)O

Technology Process of Aminoethylphosphinic acid

There total 5 articles about Aminoethylphosphinic acid 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: 49.0%

: 145728-55-8
(L,D)-1-(N-phenylacetylamino)ethylphosphinic acid

: 71937-28-5
(1R)-(-)-1-aminoethylphosphinic acid

: (S)-1-(N-phenylacetylamino)ethylphosphinic acid

Guidance literature:: With penicillin G acylase from Escherichia coli immobilized on mesoporous cellular foams; In aq. phosphate buffer; at 25 ℃; for 1h; pH=7; stereospecific reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1016/j.tetasy.2016.11.007

Reference yield: 44.0%

: 108327-37-3
[1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid

: 71937-28-5
(1R)-(-)-1-aminoethylphosphinic acid

: (S)-1-(N-benzyloxycarbonylamino)ethylphosphinic acid

Guidance literature:: With penicillin G acylase from Escherichia coli immobilized on mesoporous cellular foams; In aq. phosphate buffer; at 25 ℃; for 72h; pH=7; stereospecific reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1016/j.tetasy.2016.11.007

Reference yield: 41.0%

: 108327-37-3
[1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid

: 71937-28-5
(1R)-(-)-1-aminoethylphosphinic acid

: 115115-40-7
(R)-1-(N-benzyloxycarbonylamino)ethylphosphinic acid

: (S)-1-(N-benzyloxycarbonylamino)ethylphosphinic acid

Guidance literature:: With penicillin G acylase from Escherichia coli; In aq. phosphate buffer; at 25 ℃; for 24h; pH=7; enantioselective reaction; Kinetics; Enzymatic reaction;
DOI:10.1016/j.molcatb.2016.05.011