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Dapiramicin B

Base Information Edit
  • Chemical Name:Dapiramicin B
  • CAS No.:90044-18-1
  • Molecular Formula:C21H29N5O11
  • Molecular Weight:527.488
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60238004
  • Nikkaji Number:J111.118C
  • Wikidata:Q83120267
  • Metabolomics Workbench ID:144131
  • Mol file:90044-18-1.mol
Dapiramicin B

Synonyms:dapiramicin B

Suppliers and Price of Dapiramicin B
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
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Total 1 raw suppliers
Chemical Property of Dapiramicin B Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:914°Cat760mmHg 
  • Flash Point:506.6°C 
  • PSA:244.92000 
  • Density:1.66g/cm3 
  • LogP:-3.39872 
  • XLogP3:-3.3
  • Hydrogen Bond Donor Count:8
  • Hydrogen Bond Acceptor Count:15
  • Rotatable Bond Count:8
  • Exact Mass:527.18635676
  • Heavy Atom Count:37
  • Complexity:806
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1C(OC(C(C1O)O)OC2C(OC(C(C2O)O)NC3=NC4=C(C(=CN4)C#N)C(=N3)OC)CO)CO
  • Isomeric SMILES:CO[C@@H]1[C@H](O[C@H]([C@@H]([C@H]1O)O)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O)NC3=NC4=C(C(=CN4)C#N)C(=N3)OC)CO)CO
Technology Process of Dapiramicin B

There total 9 articles about Dapiramicin B 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:
With boron trifluoride diethyl etherate; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1016/j.tetlet.2006.06.001
Guidance literature:
Multi-step reaction with 2 steps
1: 55 percent / NaO(t-Bu) / Pd2(dba)3; (S)-BINAP / toluene / 6 h / 80 °C
2: 92 percent / BF3*OEt2 / CH2Cl2 / 0.5 h / 0 °C
With boron trifluoride diethyl etherate; sodium t-butanolate; tris(dibenzylideneacetone)dipalladium (0); (S)-(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine); In dichloromethane; toluene;
DOI:10.1016/j.tetlet.2006.06.001
Guidance literature:
Multi-step reaction with 4 steps
1: 41 percent / silicic acid; NaHCO3 / methanol; diethyl ether / sonication
2: 72 percent / SBr3; t-BuONO / various solvent(s) / 0 °C
3: 55 percent / NaO(t-Bu) / Pd2(dba)3; (S)-BINAP / toluene / 6 h / 80 °C
4: 92 percent / BF3*OEt2 / CH2Cl2 / 0.5 h / 0 °C
With tert.-butylnitrite; boron trifluoride diethyl etherate; sodium hydrogencarbonate; silicic acid; sodium t-butanolate; tris(dibenzylideneacetone)dipalladium (0); (S)-(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine); In methanol; diethyl ether; dichloromethane; toluene;
DOI:10.1016/j.tetlet.2006.06.001
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