(E)-N-morpholin-4-yl-1-[2-[(E)-2-(5-nitrothiophen-2-yl)ethenyl]-1,3-thiazol-4-yl]methanimine

Base Information

Chemical Name:(E)-N-morpholin-4-yl-1-[2-[(E)-2-(5-nitrothiophen-2-yl)ethenyl]-1,3-thiazol-4-yl]methanimine
CAS No.:56527-67-4
Molecular Formula:C14H14N4O3S2
Molecular Weight:350.416
Hs Code.:

Synonyms:(?,E)-N-((2-(2-(5-Nitro-2-thienyl)ethenyl)-4-thiazolyl)methylene)-4-morpholinamine;4-Morpholinamine, N-((2-(2-(5-nitro-2-thienyl)ethenyl)-4-thiazolyl)methylene)-, (?,E)-;56527-67-4;C14H14N4O3S2;C14-H14-N4-O3-S2;LS-92196

Suppliers and Price of (E)-N-morpholin-4-yl-1-[2-[(E)-2-(5-nitrothiophen-2-yl)ethenyl]-1,3-thiazol-4-yl]methanimine

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (E)-N-morpholin-4-yl-1-[2-[(E)-2-(5-nitrothiophen-2-yl)ethenyl]-1,3-thiazol-4-yl]methanimine

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:611.539°C at 760 mmHg
Flash Point:323.648°C
Density:1.5g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:350.05073267
Heavy Atom Count:23
Complexity:465

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1N=CC2=CSC(=N2)C=CC3=CC=C(S3)[N+](=O)[O-]
Isomeric SMILES:C1COCCN1/N=C/C2=CSC(=N2)/C=C/C3=CC=C(S3)[N+](=O)[O-]

Technology Process of (E)-N-morpholin-4-yl-1-[2-[(E)-2-(5-nitrothiophen-2-yl)ethenyl]-1,3-thiazol-4-yl]methanimine

There total 5 articles about (E)-N-morpholin-4-yl-1-[2-[(E)-2-(5-nitrothiophen-2-yl)ethenyl]-1,3-thiazol-4-yl]methanimine 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:

: 56527-72-1
3t-(5-nitro-thiophen-2-yl)-thioacrylamide

: 56527-67-4
morpholin-4-yl-{2-[trans-2-(5-nitro-thiophen-2-yl)-vinyl]-thiazol-4-ylmethylene}-amine

Guidance literature:: Multi-step reaction with 4 steps

1: dioxane

3: (i) p-NOC₆H₄NMe₂, aq. NaOH, MeOH, (ii) aq. HCl

4: AcOH / CHCl₃

With acetic acid; In 1,4-dioxane; chloroform;
DOI:10.1021/jm00242a007

Reference yield:

: 56527-75-4
1-{2-[trans-2-(5-nitro-thiophen-2-yl)-vinyl]-thiazol-4-ylmethyl}-pyridinium; chloride

: 56527-67-4
morpholin-4-yl-{2-[trans-2-(5-nitro-thiophen-2-yl)-vinyl]-thiazol-4-ylmethylene}-amine

Guidance literature:: Multi-step reaction with 2 steps

1: (i) p-NOC₆H₄NMe₂, aq. NaOH, MeOH, (ii) aq. HCl

2: AcOH / CHCl₃

With acetic acid; In chloroform;
DOI:10.1021/jm00242a007

Reference yield:

: 1-{2-[(E)-2-(5-Nitro-thiophen-2-yl)-vinyl]-thiazol-4-yl}-3,5,7-triaza-1-azonia-tricyclo[3.3.1.1^3,7]decane; chloride

: 56527-67-4
morpholin-4-yl-{2-[trans-2-(5-nitro-thiophen-2-yl)-vinyl]-thiazol-4-ylmethylene}-amine

Guidance literature:: Multi-step reaction with 2 steps

1: aq.AcOH

2: AcOH / CHCl₃

With acetic acid; In chloroform;
DOI:10.1021/jm00242a007