N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide

Base Information

Chemical Name:N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide
CAS No.:21411-19-8
Molecular Formula:C₁₈H₂₁NO₅
Molecular Weight:331.368
Hs Code.:
Mol file:21411-19-8.mol

Synonyms:

Suppliers and Price of N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide

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

TRC
N-(4-Hydroxy-3-methoxyphenethyl)-2-(3-hydroxy-4-methoxyphenyl)acetamide
2.5g
$ 1320.00

Medical Isotopes, Inc.
N-(4-Hydroxy-3-methoxyphenethyl)-2-(3-hydroxy-4-methoxyphenyl)acetamide
2.5 g
$ 2200.00

Medical Isotopes, Inc.
N-(4-Hydroxy-3-methoxyphenethyl)-2-(3-hydroxy-4-methoxyphenyl)acetamide
250 mg
$ 650.00

Total 3 raw suppliers

Chemical Property of N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide

Chemical Property:

Melting Point:124-126 °C
Boiling Point:617.1±55.0 °C(Predicted)
PKA:9.79±0.10(Predicted)
Density:1.242±0.06 g/cm3(Predicted)
Solubility.:Dimethylformamide, Methanol

Purity/Quality:

99% ^*data from raw suppliers

N-(4-Hydroxy-3-methoxyphenethyl)-2-(3-hydroxy-4-methoxyphenyl)acetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide is used in the preparation of polyphenolic tetrahydroisoquinoline alkaloids, N-norreticuline and its derivaties and phellodendrine analogs as allergy inhibitors.

Technology Process of N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide

There total 8 articles about N-(4-Hydroxy-3-Methoxyphenethyl)-2-(3-hydroxy-4-Methoxyphenyl)acetaMide 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: 90.4%

: 1131-94-8
homoisovanillic acid

: 554-52-9
3-Methoxytyramine

: 21411-19-8
N-(β-4-hydroxy-3-methoxyphenethyl)-(3-hydroxy-4-methoxyphenyl)acetamide

Guidance literature:: Heating;
DOI:10.1021/jo01292a008

Reference yield:

: 4468-59-1
4-hydroxy-3-methoxyphenylacetonitrile

: 21411-19-8
N-(β-4-hydroxy-3-methoxyphenethyl)-(3-hydroxy-4-methoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) BH₃, HCl; 2.) aqueous NH₃

2: 90.4 percent / Heating

With hydrogenchloride; ammonium hydroxide; borane;
DOI:10.1021/jo01292a008