Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate

Base Information

Chemical Name:Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate
CAS No.:918494-41-4
Molecular Formula:C17H25NO6
Molecular Weight:339.389
Hs Code.:
DSSTox Substance ID:DTXSID50582467
Wikidata:Q82473905

Synonyms:918494-41-4;Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate;DTXSID50582467

Suppliers and Price of Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:11
Exact Mass:339.16818752
Heavy Atom Count:24
Complexity:375

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)CCCCNC(=O)C1=CC(=C(C(=C1)OC)OC)OC

Technology Process of Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate

There total 3 articles about Ethyl 5-(3,4,5-trimethoxybenzamido)pentanoate 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:

: 118-41-2
Eudesmic acid

: 918494-41-4
ethyl 5-((3,4,5-trimethoxybenzoyl)amino)pentanoate

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl chloride / N,N-dimethylformamide / CH₂Cl₂

2: 3.02 g / N-ethyl-N,N-diisopropylamine / CH₂Cl₂

With oxalyl dichloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1021/jm060742o

Reference yield:

: 660-88-8
5-aminopentanoic acid

: 918494-41-4
ethyl 5-((3,4,5-trimethoxybenzoyl)amino)pentanoate

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 12 h

2: 3.02 g / N-ethyl-N,N-diisopropylamine / CH₂Cl₂

With thionyl chloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jm060742o