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9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine

Base Information Edit
  • Chemical Name:9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine
  • CAS No.:85421-87-0
  • Molecular Formula:C32H23N7O13S
  • Molecular Weight:745.64
  • Hs Code.:
  • Mol file:85421-87-0.mol
9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine

Synonyms:9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine

Suppliers and Price of 9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine Edit
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MSDS Files:

SDS file from LookChem

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Technology Process of 9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine

There total 4 articles about 9-<6'-deoxy-2',3',5'-tris-O-(p-nitrobenzoyl)-β-D-allofuranosyl>-6-thiopurine 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 2 steps
1: 85 percent / mercuric cyanide, mercuric bromide, / 1,2-dichloro-ethane / Ambient temperature
2: 100 percent / thiourea / ethanol / 4 h / Heating
With mercury(II) cyanide; thiourea; mercury dibromide; In ethanol; 1,2-dichloro-ethane;
DOI:10.1021/jm00361a023
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / mercuric cyanide, mercuric bromide, / 1,2-dichloro-ethane / Ambient temperature
2: 100 percent / thiourea / ethanol / 4 h / Heating
With mercury(II) cyanide; thiourea; mercury dibromide; In ethanol; 1,2-dichloro-ethane;
DOI:10.1021/jm00361a023
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