5-[[1,3-benzodioxol-5-ylmethyl-[(3,4-dimethoxyphenyl)methyl]amino]methyl]-N-hexylfuran-2-carboxamide

Base Information

Chemical Name:5-[[1,3-benzodioxol-5-ylmethyl-[(3,4-dimethoxyphenyl)methyl]amino]methyl]-N-hexylfuran-2-carboxamide
CAS No.:5933-16-4
Molecular Formula:C₁₄H₁₉NO
Molecular Weight:217.311
Hs Code.:
DSSTox Substance ID:DTXSID00974752
Wikidata:Q82959200

Synonyms:5933-16-4;DTXSID00974752;5-({[(2H-1,3-Benzodioxol-5-yl)methyl][(3,4-dimethoxyphenyl)methyl]amino}methyl)-N-hexylfuran-2-carboxamide

Suppliers and Price of 5-[[1,3-benzodioxol-5-ylmethyl-[(3,4-dimethoxyphenyl)methyl]amino]methyl]-N-hexylfuran-2-carboxamide

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

Total 0 raw suppliers

Chemical Property of 5-[[1,3-benzodioxol-5-ylmethyl-[(3,4-dimethoxyphenyl)methyl]amino]methyl]-N-hexylfuran-2-carboxamide

Chemical Property:

Vapor Pressure:3.43E-15mmHg at 25°C
Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
XLogP3:5.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:14
Exact Mass:508.25733687
Heavy Atom Count:37
Complexity:681

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCNC(=O)C1=CC=C(O1)CN(CC2=CC3=C(C=C2)OCO3)CC4=CC(=C(C=C4)OC)OC

Technology Process of 5-[[1,3-benzodioxol-5-ylmethyl-[(3,4-dimethoxyphenyl)methyl]amino]methyl]-N-hexylfuran-2-carboxamide

There total 2 articles about 5-[[1,3-benzodioxol-5-ylmethyl-[(3,4-dimethoxyphenyl)methyl]amino]methyl]-N-hexylfuran-2-carboxamide 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:

: 2978-58-7
1,1-dimethylprop-3-ynylamine

: 5933-16-4
2-(1,1-dimethyl-but-2-ynylamino)-1-phenyl-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: (i) NaNH₂, liq. NH₃, Et₂O, (ii) /BRN= 969135/

DOI:10.1021/jo01339a026

Reference yield:

: 96-09-3
styrene oxide

: 31914-32-6
1,1-dimethyl-2-butynylamine

: 5933-16-4
2-(1,1-dimethyl-but-2-ynylamino)-1-phenyl-ethanol

Guidance literature:: DOI:10.1021/jo01339a026

Reference yield:

: 5933-16-4
2-(1,1-dimethyl-but-2-ynylamino)-1-phenyl-ethanol

: 5992-97-2
5,5,7-trimethyl-2-phenyl-[1,4]oxazepane

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / xylene / 4 h / Heating

2: H₂ / Pd-C / ethanol / 16 h / Ambient temperature

With potassium hydroxide; hydrogen; palladium on activated charcoal; In ethanol; xylene;
DOI:10.1021/jo01339a026