RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYL PHOSPHOCHOLINE

Base Information

Chemical Name:RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYL PHOSPHOCHOLINE
CAS No.:112989-01-2
Molecular Formula:C₂₆H₅₅N₂O₆P
Molecular Weight:522.706
Hs Code.:
Mol file:112989-01-2.mol

Synonyms:3,5-Dioxa-9-aza-4-phosphapentacosan-1-aminium,7-ethoxy-4-hydroxy-N,N,N-trimethyl-10-oxo-, inner salt, 4-oxide, (?à)-

Suppliers and Price of RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYL PHOSPHOCHOLINE

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

American Custom Chemicals Corporation
RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYLPHOSPHOCHOLINE 95.00%
5MG
$ 500.32

Total 2 raw suppliers

Chemical Property of RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYL PHOSPHOCHOLINE

Chemical Property:

PSA：106.73000
LogP:6.65790
Storage Temp.:−20°C

Purity/Quality:

95% ^*data from raw suppliers

RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYLPHOSPHOCHOLINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYL PHOSPHOCHOLINE

There total 8 articles about RAC-2-ETHOXY-3-HEXADECANAMIDO-1-PROPYL PHOSPHOCHOLINE 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:

: 112988-88-2
(+/-)-3-hexadecanamido-1,2-propanediol

: 112989-01-2
rac-2-ethoxy-3-hexadecanamido-1-propylphosphocholine

Guidance literature:: Multi-step reaction with 5 steps

1.1: 53 percent / pyridine / 10 h / 45 - 50 °C

2.1: NaH / tetrahydrofuran / 1 h / 20 °C

2.2: tetrahydrofuran / 4 h / 50 °C

3.1: p-TsOH; MeOH / CH₂Cl₂ / 8 h / 20 °C

4.1: pyridine / diethyl ether; tetrahydrofuran / 4 h / Heating

4.2: H₂O; pyridine / diethyl ether; tetrahydrofuran / 1 h

5.1: CHCl₃; propan-2-ol; various solvent(s) / 5 h / 65 °C

With pyridine; methanol; sodium hydride; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; dichloromethane; chloroform; isopropyl alcohol;
DOI:10.1021/jm020001x

Reference yield:

: 112988-90-6
(+/-)-3-hexadecanamido-1(triphenylmethoxy)-2-propanol

: 112989-01-2
rac-2-ethoxy-3-hexadecanamido-1-propylphosphocholine

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaH / tetrahydrofuran / 1 h / 20 °C

1.2: tetrahydrofuran / 4 h / 50 °C

2.1: p-TsOH; MeOH / CH₂Cl₂ / 8 h / 20 °C

3.1: pyridine / diethyl ether; tetrahydrofuran / 4 h / Heating

3.2: H₂O; pyridine / diethyl ether; tetrahydrofuran / 1 h

4.1: CHCl₃; propan-2-ol; various solvent(s) / 5 h / 65 °C

With pyridine; methanol; sodium hydride; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; dichloromethane; chloroform; isopropyl alcohol;
DOI:10.1021/jm020001x

Reference yield:

: 112988-93-9
(+/-)-3-hexadecanamido-2-ethoxy-1-(triphenylmethoxy)propane

: 112989-01-2
rac-2-ethoxy-3-hexadecanamido-1-propylphosphocholine

Guidance literature:: Multi-step reaction with 3 steps

1.1: p-TsOH; MeOH / CH₂Cl₂ / 8 h / 20 °C

2.1: pyridine / diethyl ether; tetrahydrofuran / 4 h / Heating

2.2: H₂O; pyridine / diethyl ether; tetrahydrofuran / 1 h

3.1: CHCl₃; propan-2-ol; various solvent(s) / 5 h / 65 °C

With pyridine; methanol; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; dichloromethane; chloroform; isopropyl alcohol;
DOI:10.1021/jm020001x