N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine

Base Information

Chemical Name:N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine
CAS No.:31968-01-1
Molecular Formula:C₁₂H₁₂N₄O₄S
Molecular Weight:308.318
Hs Code.:
ChEMBL ID:CHEMBL3273837
Mol file:31968-01-1.mol

Synonyms:BRN 0566062;31968-01-1;N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine;4-Morpholinamine, N-((2-(5-nitro-2-furanyl)-4-thiazolyl)methylene)-;N-((2-(5-Nitrofuran-2-yl)thiazol-4-yl)methylene)morpholin-4-amine;CHEMBL3273837;LS-92195

Suppliers and Price of N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine

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 N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:544.902°C at 760 mmHg
Flash Point:283.347°C
Density:1.594g/cm³
XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:308.05792605
Heavy Atom Count:21
Complexity:399

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1N=CC2=CSC(=N2)C3=CC=C(O3)[N+](=O)[O-]
Isomeric SMILES:C1COCCN1/N=C/C2=CSC(=N2)C3=CC=C(O3)[N+](=O)[O-]

Technology Process of N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine

There total 6 articles about N-((2-(5-Nitro-2-furanyl)-4-thiazolyl)methylene)-4-morpholinamine 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:

: 59-84-7
5-nitrofuran-2-carbothioamide

: 31968-01-1
morpholin-4-yl-[2-(5-nitro-furan-2-yl)-thiazol-4-ylmethylene]-amine

Guidance literature:: Multi-step reaction with 5 steps

1: dimethylformamide

2: dimethylformamide

3: aq. HCl / dioxane

4: Na₂Cr₂O₇*2H₂O / acetic acid

5: AcOH / CHCl₃

With hydrogenchloride; sodium dichromate; acetic acid; In 1,4-dioxane; chloroform; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00217a017

Reference yield:

: 31898-51-8
[2-(5-nitro-furan-2-yl)-thiazol-4-yl]-methanol

: 31968-01-1
morpholin-4-yl-[2-(5-nitro-furan-2-yl)-thiazol-4-ylmethylene]-amine

Guidance literature:: Multi-step reaction with 2 steps

1: Na₂Cr₂O₇*2H₂O / acetic acid

2: AcOH / CHCl₃

With sodium dichromate; acetic acid; In chloroform; acetic acid;
DOI:10.1021/jm00217a017

Reference yield:

: 13218-17-2
4-chloromethyl-2-(5-nitro-furan-2-yl)-thiazole

: 31968-01-1
morpholin-4-yl-[2-(5-nitro-furan-2-yl)-thiazol-4-ylmethylene]-amine

Guidance literature:: Multi-step reaction with 4 steps

1: dimethylformamide

2: aq. HCl / dioxane

3: Na₂Cr₂O₇*2H₂O / acetic acid

4: AcOH / CHCl₃

With hydrogenchloride; sodium dichromate; acetic acid; In 1,4-dioxane; chloroform; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00217a017