N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide

Base Information

Chemical Name:N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide
CAS No.:918494-53-8
Molecular Formula:C15H23N3O5
Molecular Weight:325.365
Hs Code.:
DSSTox Substance ID:DTXSID70582469
Wikidata:Q82473907

Synonyms:918494-53-8;N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide;DTXSID70582469

Suppliers and Price of N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide

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 N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide

Chemical Property:

XLogP3:0.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:325.16377084
Heavy Atom Count:23
Complexity:366

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)C(=O)NCCCCC(=O)NN

Technology Process of N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide

There total 5 articles about N-(5-Hydrazinyl-5-oxopentyl)-3,4,5-trimethoxybenzamide 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: 71.0%

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

: 918494-53-8
N-(5-hydrazino-5-oxopentyl)-3,4,5-trimethoxybenzamide

Guidance literature:: With hydrazine hydrate; In ethanol; for 24h; Heating;
DOI:10.1021/jm060742o

Reference yield:

: 118-41-2
Eudesmic acid

: 918494-53-8
N-(5-hydrazino-5-oxopentyl)-3,4,5-trimethoxybenzamide

Guidance literature:: Multi-step reaction with 3 steps

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

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

3: 71 percent / hydrazine hydrate / ethanol / 24 h / Heating

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

Reference yield:

: 29840-57-1
5-aminovaleric acid ethyl ester hydrochloride

: 918494-53-8
N-(5-hydrazino-5-oxopentyl)-3,4,5-trimethoxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 3.02 g / N-ethyl-N,N-diisopropylamine / CH₂Cl₂

2: 71 percent / hydrazine hydrate / ethanol / 24 h / Heating

With hydrazine hydrate; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane;
DOI:10.1021/jm060742o