N-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide

Base Information

Chemical Name:N-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide
CAS No.:56527-68-5
Molecular Formula:C12H12N4O4S3
Molecular Weight:372.4431
Hs Code.:

Synonyms:BRN 1043595;N-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide;4-Thiomorpholinamine, N-((2-(5-nitro-2-thienyl)-4-thiazolyl)methylene)-, 1,1-dioxide;56527-68-5;LS-152754

Suppliers and Price of N-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide

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-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:705.1°Cat760mmHg
Flash Point:380.3°C
Density:1.73g/cm³
XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:3
Exact Mass:372.00206840
Heavy Atom Count:23
Complexity:560

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CS(=O)(=O)CCN1N=CC2=CSC(=N2)C3=CC=C(S3)[N+](=O)[O-]
Isomeric SMILES:C1CS(=O)(=O)CCN1/N=C/C2=CSC(=N2)C3=CC=C(S3)[N+](=O)[O-]

Technology Process of N-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide

There total 6 articles about N-((2-(5-Nitro-2-thienyl)-4-thiazolyl)methylene)-4-thiomorpholinamine 1,1-dioxide 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:

: 30096-68-5
5-nitro-thiophene-2-carbothioic acid amide

: 56527-68-5
(1,1-dioxo-1λ⁶-thiomorpholin-4-yl)-[2-(5-nitro-thiophen-2-yl)-thiazol-4-ylmethylene]-amine

Guidance literature:: Multi-step reaction with 4 steps

1: dioxane

2: CHCl₃

3: aq. AcOH

4: AcOH / CHCl₃

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

Reference yield:

: 42344-00-3
4-chloromethyl-2-(5-nitro-thiophen-2-yl)-thiazole

: 56527-68-5
(1,1-dioxo-1λ⁶-thiomorpholin-4-yl)-[2-(5-nitro-thiophen-2-yl)-thiazol-4-ylmethylene]-amine

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃

2: aq. AcOH

3: AcOH / CHCl₃

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

Reference yield:

: 31898-36-9
N,N-dimethyl-N'-[2-(5-nitro-thiophen-2-yl)-thiazol-4-ylmethylene]-benzene-1,4-diamine N'-oxide

: 56527-68-5
(1,1-dioxo-1λ⁶-thiomorpholin-4-yl)-[2-(5-nitro-thiophen-2-yl)-thiazol-4-ylmethylene]-amine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HCl

2: AcOH / CHCl₃

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