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4'-Demethylamino-4'-hydroxystaurosporine

Base Information Edit
  • Chemical Name:4'-Demethylamino-4'-hydroxystaurosporine
  • CAS No.:126572-73-4
  • Molecular Formula:C27H23 N3 O4
  • Molecular Weight:453.49
  • Hs Code.:
  • Nikkaji Number:J1.319.181F
  • Wikidata:Q77502285
  • Metabolomics Workbench ID:107897
  • ChEMBL ID:CHEMBL4762923
  • Mol file:126572-73-4.mol
4'-Demethylamino-4'-hydroxystaurosporine

Synonyms:4'-demethylamino-4'-hydroxy-staurosporine;4'-demethylamino-4'-hydroxystaurosporine;RK 286C;RK-286C

Suppliers and Price of 4'-Demethylamino-4'-hydroxystaurosporine
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
  • price
  • American Custom Chemicals Corporation
  • 4'-DEMETHYLAMINO-4'-HYDROXYSTAUROSPORINE 95.00%
  • 5MG
  • $ 497.16
Total 2 raw suppliers
Chemical Property of 4'-Demethylamino-4'-hydroxystaurosporine Edit
Chemical Property:
  • Boiling Point:707.4°Cat760mmHg 
  • PKA:13.79±0.60(Predicted) 
  • Flash Point:381.6°C 
  • PSA:81.14000 
  • Density:1.64g/cm3 
  • LogP:4.13730 
  • XLogP3:3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:453.16885622
  • Heavy Atom Count:34
  • Complexity:886
Purity/Quality:

99%min *data from raw suppliers

4'-DEMETHYLAMINO-4'-HYDROXYSTAUROSPORINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12C(C(CC(O1)N3C4=CC=CC=C4C5=C6C(=C7C8=CC=CC=C8N2C7=C53)CNC6=O)O)OC
  • Isomeric SMILES:C[C@@]12[C@@H]([C@@H](C[C@@H](O1)N3C4=CC=CC=C4C5=C6C(=C7C8=CC=CC=C8N2C7=C53)CNC6=O)O)OC
Technology Process of 4'-Demethylamino-4'-hydroxystaurosporine

There total 14 articles about 4'-Demethylamino-4'-hydroxystaurosporine 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 methoxybenzene; trifluoroacetic acid;
DOI:10.1021/ja9626143
Guidance literature:
With potassium tri-sec-butyl-borohydride;
DOI:10.7164/antibiotics.53.426
Guidance literature:
Multi-step reaction with 6 steps
1: 89 percent / LiBH4 / tetrahydrofuran / 0.33 h
2: 71 percent / pyridinium trifluoroacetate, 1,3-dicyclohexylcarbodiimide / benzene; dimethylsulfoxide / 9 h / Ambient temperature
3: 85 percent / BF3*OEt2 / diethyl ether / 24 h / 25 - 30 °C
4: 95 percent / NaBH4 / methanol; CH2Cl2; CHCl3 / 0.08 h
5: 1.) NaH / 1) THF, 25 min; 2) THF, 50 min
6: 75 percent / TFA, thioanisole / 24 h
With sodium tetrahydroborate; lithium borohydride; methyl-phenyl-thioether; boron trifluoride diethyl etherate; pyridinium trifluroacetate; sodium hydride; dicyclohexyl-carbodiimide; trifluoroacetic acid; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; chloroform; dimethyl sulfoxide; benzene;
DOI:10.1021/ja971304x
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