Serine ethanolamine phosphate

Base Information

Chemical Name:Serine ethanolamine phosphate
CAS No.:1186-34-1
Molecular Formula:C5H13 N2 O6 P
Molecular Weight:228.142
Hs Code.:2931900090
Mol file:1186-34-1.mol

Synonyms:serine ethanolamine phosphate;serine ethanolamine phosphate, (D)-isomer;serine ethanolamine phosphodiester

Suppliers and Price of Serine ethanolamine phosphate

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 6 raw suppliers

Chemical Property of Serine ethanolamine phosphate

Chemical Property:

Vapor Pressure:6.77E-09mmHg at 25°C
Boiling Point:438°C at 760 mmHg
Flash Point:218.7°C
PSA：154.91000
Density:1.543g/cm³
LogP:-0.10880
XLogP3:-7.8
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:7
Exact Mass:228.05112314
Heavy Atom Count:14
Complexity:234

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(COP(=O)(O)OCC(C(=O)O)N)N

Technology Process of Serine ethanolamine phosphate

There total 2 articles about Serine ethanolamine phosphate 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:

: 21209-51-8
N-benzyloxycarbonyl-L-serine benzyl ester

: 770-12-7
O-phenyl phosphorodichloridate

: 1186-34-1
L-serine ethanolamine phosphate

: 2643-42-7
O,O'-hydroxyphosphoryl-di-L-serine

Guidance literature:: With quinoline; anschliessend mit 2-Benzyloxycarbonylamino-aethanol und Pyridin in CHCl₃ und Hydrieren des Reaktionsprodukts an Palladium/Kohle und an Platin;
DOI:10.1021/ja01592a018