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[Ru(4,7-diphenyl-1,10-phenanthroline)(SCN)2(4-(6-oxo-[1,10]phenanthroline-5-ylideneamino)-3-hydroxynaphthalene-1-sulfonic acid)]

Base Information Edit
  • Chemical Name:[Ru(4,7-diphenyl-1,10-phenanthroline)(SCN)2(4-(6-oxo-[1,10]phenanthroline-5-ylideneamino)-3-hydroxynaphthalene-1-sulfonic acid)]
  • CAS No.:1612890-70-6
  • Molecular Formula:C48H29N7O5RuS3
  • Molecular Weight:981.07
  • Hs Code.:
  • Mol file:1612890-70-6.mol
[Ru(4,7-diphenyl-1,10-phenanthroline)(SCN)2(4-(6-oxo-[1,10]phenanthroline-5-ylideneamino)-3-hydroxynaphthalene-1-sulfonic acid)]

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of [Ru(4,7-diphenyl-1,10-phenanthroline)(SCN)2(4-(6-oxo-[1,10]phenanthroline-5-ylideneamino)-3-hydroxynaphthalene-1-sulfonic acid)] Edit
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Technology Process of [Ru(4,7-diphenyl-1,10-phenanthroline)(SCN)2(4-(6-oxo-[1,10]phenanthroline-5-ylideneamino)-3-hydroxynaphthalene-1-sulfonic acid)]

There total 3 articles about [Ru(4,7-diphenyl-1,10-phenanthroline)(SCN)2(4-(6-oxo-[1,10]phenanthroline-5-ylideneamino)-3-hydroxynaphthalene-1-sulfonic acid)] 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:
Guidance literature:
Multi-step reaction with 4 steps
1: potassium bromide; sulfuric acid; nitric acid / 4 h / Reflux
2: ethanol / 4 h / Reflux
3: 4 h / Inert atmosphere; Reflux
4: ethanol / 4 h / Inert atmosphere; Reflux
With sulfuric acid; nitric acid; potassium bromide; In ethanol;
DOI:10.1039/c3dt52949e
Guidance literature:
Multi-step reaction with 3 steps
1: ethanol / 4 h / Reflux
2: 4 h / Inert atmosphere; Reflux
3: ethanol / 4 h / Inert atmosphere; Reflux
In ethanol;
DOI:10.1039/c3dt52949e
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