N-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea

Base Information

Chemical Name:N-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea
CAS No.:87653-56-3
Molecular Formula:C₂₂H₃₂N₄O₂
Molecular Weight:384.522
Hs Code.:
DSSTox Substance ID:DTXSID70539998
Wikidata:Q82415853

Synonyms:87653-56-3;DTXSID70539998;N-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea

Suppliers and Price of N-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea

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-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:12
Exact Mass:384.25252628
Heavy Atom Count:28
Complexity:539

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC(=O)NCCCCCCCCCCN1C(=O)C=CC(=N1)C2=CC=CC=C2

Technology Process of N-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea

There total 3 articles about N-Methyl-N'-[10-(6-oxo-3-phenylpyridazin-1(6H)-yl)decyl]urea 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:

: 2166-31-6
6-phenylpyridazin-3(2H)-one

: 87653-56-3
1-Methyl-3-[10-(6-oxo-3-phenyl-6H-pyridazin-1-yl)-decyl]-urea

Guidance literature:: Multi-step reaction with 3 steps

1: 49 percent / potassium hydroxide, tetra-n-butylammonium bromide / benzene / 6 h / Ambient temperature

2: 49 percent / 25percent ammonium hydroxide / ethanol / 24 h / 40 °C

3: 34 percent / CHCl₃

With potassium hydroxide; ammonium hydroxide; tetrabutylammomium bromide; In ethanol; chloroform; benzene;

Reference yield:

: 4101-68-2
1,10-dibromodecane

: 87653-56-3
1-Methyl-3-[10-(6-oxo-3-phenyl-6H-pyridazin-1-yl)-decyl]-urea

Guidance literature:: Multi-step reaction with 3 steps

1: 49 percent / potassium hydroxide, tetra-n-butylammonium bromide / benzene / 6 h / Ambient temperature

2: 49 percent / 25percent ammonium hydroxide / ethanol / 24 h / 40 °C

3: 34 percent / CHCl₃

With potassium hydroxide; ammonium hydroxide; tetrabutylammomium bromide; In ethanol; chloroform; benzene;

Reference yield:

: 87653-64-3
2-(2-bromodecyl)-6-phenyl-3(2H)-pyridazinone

: 87653-56-3
1-Methyl-3-[10-(6-oxo-3-phenyl-6H-pyridazin-1-yl)-decyl]-urea

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / 25percent ammonium hydroxide / ethanol / 24 h / 40 °C

2: 34 percent / CHCl₃

With ammonium hydroxide; In ethanol; chloroform;