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Mitomycin B

Base Information
  • Chemical Name:Mitomycin B
  • CAS No.:4055-40-7
  • Molecular Formula:C16H19 N3 O6
  • Molecular Weight:349.343
  • Hs Code.:
  • UNII:VT1IGL3D7V
  • DSSTox Substance ID:DTXSID001318185
  • Nikkaji Number:J55.724B
  • Wikidata:Q22252155
  • NCI Thesaurus Code:C1392
  • Metabolomics Workbench ID:102726
  • ChEMBL ID:CHEMBL323536
  • Mol file:4055-40-7.mol
Mitomycin B

Synonyms:mitomycin A;mitomycin A, (1aS-(1aalpha,8alpha,8aalpha,8balpha))-isomer;mitomycin B

Suppliers and Price of Mitomycin B
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
  • American Custom Chemicals Corporation
  • MITOMYCIN B 95.00%
  • 1MG
  • $ 479.85
Total 21 raw suppliers
Chemical Property of Mitomycin B
Chemical Property:
  • Refractive Index:1.6500 (estimate) 
  • Boiling Point:606.6°Cat760mmHg 
  • PKA:11.41±0.70(Predicted) 
  • Flash Point:320.6°C 
  • PSA:122.17000 
  • Density:1.57g/cm3 
  • LogP:-0.69930 
  • XLogP3:-0.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:4
  • Exact Mass:349.12738533
  • Heavy Atom Count:25
  • Complexity:787
Purity/Quality:

98%Min *data from raw suppliers

MITOMYCIN B 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Chemical Classes:Biological Agents -> Bacterial Toxins
  • Canonical SMILES:CC1=C(C(=O)C2=C(C1=O)N3CC4C(C3(C2COC(=O)N)O)N4C)OC
  • Isomeric SMILES:CC1=C(C(=O)C2=C(C1=O)N3C[C@H]4[C@@H]([C@@]3([C@H]2COC(=O)N)O)N4C)OC
  • Uses As an antitumor antibiotic, Mitomycin B is used as antineoplastic.
Technology Process of Mitomycin B

There total 1 articles about Mitomycin 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 oxygen; In ethanol;
DOI:10.1021/ja00333a056
Guidance literature:
With triethylamine; In methanol; for 10h; Ambient temperature;
DOI:10.7164/antibiotics.46.1428
Guidance literature:
With sodium hydroxide; at 20 ℃; for 2h;
DOI:10.1021/ja0700193
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