6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine

Base Information

Chemical Name:6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine
CAS No.:121041-55-2
Molecular Formula:C₁₁H₁₀N₄O₂S
Molecular Weight:262.292
Hs Code.:
DSSTox Substance ID:DTXSID80567242
Wikidata:Q82453060
Mol file:121041-55-2.mol

Synonyms:121041-55-2;6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine;SCHEMBL10480613;DTXSID80567242;6-((3-Nitrobenzyl)thio)pyridazin-3-amine

Suppliers and Price of 6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine

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 6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:262.05244675
Heavy Atom Count:18
Complexity:287

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)[N+](=O)[O-])CSC2=NN=C(C=C2)N

Technology Process of 6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine

There total 1 articles about 6-{[(3-Nitrophenyl)methyl]sulfanyl}pyridazin-3-amine 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:

: 5788-46-5
6-aminopyridazine-3-thiol

: 619-23-8
3-Nitrobenzyl chloride

: 121041-55-2
6-(3'-nitrobenzylthio)pyridazin-3-amine

Guidance literature:: With sodium hydroxide;

Reference yield:

: 121041-55-2
6-(3'-nitrobenzylthio)pyridazin-3-amine

: 3-benzamidomethyl-6-(3'-nitrobenzylthio)-2-styrylimidazo<1,2-b>pyridazine

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) NaHCO₃ / 1.) EtOH, reflux, 2.) EtOH, reflux

2: 18 percent / conc. H₂SO₄ / acetic acid / 120 °C

With sulfuric acid; sodium hydrogencarbonate; In acetic acid;

Reference yield:

: 121041-55-2
6-(3'-nitrobenzylthio)pyridazin-3-amine

: 6-(3'-aminobenzylthio)-3-methoxy-2-phenylimidazo<1,2-b>pyridazine

Guidance literature:: Multi-step reaction with 3 steps

1: conc. HCl / ethanol / 9 h / Heating

2: 0.060 g / diethyl ether

3: 0.030 g / Fe, HCl, H₂O / methanol / 1.5 h / 85 - 90 °C

With hydrogenchloride; water; iron; In methanol; diethyl ether; ethanol;