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Macbecin

Base Information
  • Chemical Name:Macbecin
  • CAS No.:73341-72-7
  • Molecular Formula:C30H42N2O8
  • Molecular Weight:558.672
  • Hs Code.:
  • UNII:GB3Z258LF8
  • Wikipedia:Macbecin
  • ChEMBL ID:CHEMBL523493
  • Mol file:73341-72-7.mol
Macbecin

Synonyms:geldanamycin, 6,17-didemethoxy-15-methoxy-6-methyl-11-O-methyl-, (6S,15R)-;macbecin I

Suppliers and Price of Macbecin
Supply Marketing:
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
  • Usbiological
  • Macbecin I
  • 1mg
  • $ 573.00
  • TRC
  • MacbecinI
  • 0.5mg
  • $ 1200.00
  • Tocris
  • MacbecinI
  • 1
  • $ 311.00
  • Cayman Chemical
  • Macbecin I ≥95%
  • 1mg
  • $ 259.00
  • ApexBio Technology
  • MacbecinI
  • 1mg
  • $ 465.00
  • American Custom Chemicals Corporation
  • MACBECIN I 95.00%
  • 5G
  • $ 1928.08
  • American Custom Chemicals Corporation
  • MACBECIN I 95.00%
  • 2.5G
  • $ 1473.14
  • American Custom Chemicals Corporation
  • MACBECIN I 95.00%
  • 1G
  • $ 983.52
Total 8 raw suppliers
Chemical Property of Macbecin
Chemical Property:
  • Vapor Pressure:1.55E-21mmHg at 25°C 
  • Melting Point:205-206 °C(Solv: ethanol (64-17-5); water (7732-18-5)) 
  • Boiling Point:736.2°C at 760 mmHg 
  • PKA:8.62±0.70(Predicted) 
  • Flash Point:399°C 
  • PSA:143.25000 
  • Density:1.17g/cm3 
  • LogP:4.36350 
  • Storage Temp.:Desiccate at -20°C 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:5
  • Exact Mass:558.29411630
  • Heavy Atom Count:40
  • Complexity:1130
Purity/Quality:

99% *data from raw suppliers

Macbecin I *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CC(C(C(C=C(C(C(C=CC=C(C(=O)NC2=CC(=O)C=C(C1OC)C2=O)C)C)OC(=O)N)C)C)OC)OC
  • Isomeric SMILES:C[C@H]1C[C@@H]([C@@H]([C@H](/C=C(/[C@@H]([C@H](/C=C\C=C(\C(=O)NC2=CC(=O)C=C([C@@H]1OC)C2=O)/C)C)OC(=O)N)\C)C)OC)OC
  • Uses Macbecin I is an ansamycin antibiotic inhibitor of Hsp90 activity.
Technology Process of Macbecin

There total 113 articles about Macbecin 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 trifluoroacetic acid; In dichloromethane; at 0 - 25 ℃; for 3h;
DOI:10.1039/P19900000047
Guidance literature:
With ammonium cerium(IV) nitrate; In water; acetonitrile; at 0 ℃; for 0.133333h;
DOI:10.1039/P19900000047
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