N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

Base Information

Chemical Name:N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide
CAS No.:99254-56-5
Molecular Formula:C₂₁H₂₆INO₄
Molecular Weight:483.346
Hs Code.:

Synonyms:N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

Suppliers and Price of N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

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Technology Process of N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

There total 2 articles about N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide 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: 100.0%

: 3490-06-0
N-methylhomoveratrylamine

: 99254-55-4
2-iodo-5-methoxybenzenepropanoyl chloride

: 99254-56-5
N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

Guidance literature:: In N,N-dimethyl-formamide; for 3h; Ambient temperature;
DOI:10.1021/jm00398a023

Reference yield:

: 99254-50-9
β-(2-iodo-5-methoxyphenyl)propionic acid

: 99254-56-5
N-<2-(3,4-dimethoxyphenyl)ethyl>-2-iodo-5-methoxy-N-methylbenzenepropanamide

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl chloride / dimethylformamide / 16 h / Ambient temperature

2: 100 percent / dimethylformamide / 3 h / Ambient temperature

With oxalyl dichloride; In N,N-dimethyl-formamide;
DOI:10.1021/jm00398a023