DepropylaMino Hydroxy Propafenone

Base Information

Chemical Name:DepropylaMino Hydroxy Propafenone
CAS No.:91401-73-9
Molecular Formula:C₁₈H₂₀O₄
Molecular Weight:300.354
Hs Code.:
Mol file:91401-73-9.mol

Synonyms:DepropylaMino Hydroxy Propafenone;1-[2-(2,3-Dihydroxypropoxy)phenyl]-3-phenyl-1-propanone;Despropylamino Hydroxy Propafenone

Suppliers and Price of DepropylaMino Hydroxy Propafenone

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

Usbiological
Depropylamino Hydroxy Propafenone
25mg
$ 460.00

TRC
DepropylaminoHydroxyPropafenone
100mg
$ 640.00

Biosynth Carbosynth
1-[2-(2,3-Dihydroxypropoxy)phenyl]-3-phenyl-1-propanone
250 mg
$ 1640.00

Biosynth Carbosynth
1-[2-(2,3-Dihydroxypropoxy)phenyl]-3-phenyl-1-propanone
100 mg
$ 901.00

Biosynth Carbosynth
1-[2-(2,3-Dihydroxypropoxy)phenyl]-3-phenyl-1-propanone
50 mg
$ 496.00

Biosynth Carbosynth
1-[2-(2,3-Dihydroxypropoxy)phenyl]-3-phenyl-1-propanone
25 mg
$ 272.50

Biosynth Carbosynth
1-[2-(2,3-Dihydroxypropoxy)phenyl]-3-phenyl-1-propanone
10 mg
$ 149.90

Total 12 raw suppliers

Chemical Property of DepropylaMino Hydroxy Propafenone

Chemical Property:

PSA：66.76000
LogP:2.23410
Storage Temp.:-20°C Freezer
Solubility.:Chloroform, Ethyl Acetate

Purity/Quality:

97% ^*data from raw suppliers

Depropylamino Hydroxy Propafenone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Depropylamino Hydroxy Propafenone (Propafenone EP Impurity D) is a metabolite of the sodium channel blocker Propafenone (P757500). A metabolite of the sodium channel blocker Propafenone (P757500).

Technology Process of DepropylaMino Hydroxy Propafenone

There total 7 articles about DepropylaMino Hydroxy Propafenone 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: 85.0%

: 189766-46-9
(S)-2,2-dimethyl-4-{2-[2-(2-phenylethyl)-1,3-dioxolan-2-yl]phenoxymethyl}-1,3-dioxolane

: 189766-47-0,91401-73-9
1-[2-((R)-2,3-Dihydroxy-propoxy)-phenyl]-3-phenyl-propan-1-one

Guidance literature:: With hydrogenchloride; In acetonitrile; at 50 ℃; for 1h;
DOI:10.1007/BF00807638

Reference yield: 10.0%

: 22525-95-7
1-(2-(oxiran-2-ylmethoxy)phenyl)-3-phenylpropan-1-one

: 91401-73-9
2-(2',3'-dihydroxy-propoxy)-ω-phenyl-propiophenone

Guidance literature:: With sulfuric acid; In tetrahydrofuran; at 70 ℃; for 14h;

Reference yield:

: 118-93-4,104809-67-8
o-hydroxyacetophenone

: 91401-73-9
2-(2',3'-dihydroxy-propoxy)-ω-phenyl-propiophenone

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) 50percent NaOH, 2.) H₂ / 2.) Pd-charcoal / 1.) methanol, r.t., 60 h, 2.) methanol, normal pressure

3: 10 percent / 1N H₂SO₄ / tetrahydrofuran / 14 h / 70 °C

With sodium hydroxide; sulfuric acid; hydrogen; palladium on activated charcoal; In tetrahydrofuran;