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Technology Process of Azinomycin B

Azinomycin B

Base Information
  • Chemical Name:Azinomycin B
  • CAS No.:106486-76-4
  • Deprecated CAS:81553-83-5,1403-29-8,1403-28-7,1403-26-5
  • Molecular Formula:C31H33 N3 O11
  • Molecular Weight:623.612
  • Hs Code.:
  • UNII:051R55X44C
  • DSSTox Substance ID:DTXSID9040421
  • Metabolomics Workbench ID:57556
  • Nikkaji Number:J81.917D
  • Wikidata:Q27236057,Q20164387
  • Wikipedia:Azinomycin_B
  • Mol file:106486-76-4.mol
Azinomycin B

Synonyms:azinomycin B

Suppliers and Price of Azinomycin 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
  • AZINOMYCIN B 95.00%
  • 5MG
  • $ 497.73
Total 1 raw suppliers
Chemical Property of Azinomycin B
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:190° (dec) 
  • Boiling Point:912.3°Cat760mmHg 
  • Flash Point:505.6°C 
  • PSA：200.08000 
  • Density:1.48g/cm3 
  • LogP:2.51240 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:12
  • Rotatable Bond Count:12
  • Exact Mass:623.21150888
  • Heavy Atom Count:45
  • Complexity:1310
Purity/Quality:

AZINOMYCIN B 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C2C=C(C=C(C2=CC=C1)C(=O)OC(C(=O)NC(=C3C(C(C4N3C4)O)OC(=O)C)C(=O)NC(=CO)C(=O)C)C5(CO5)C)OC
  • Isomeric SMILES:CC1=C2C=C(C=C(C2=CC=C1)C(=O)O[C@H](C(=O)N/C(=C/3\[C@H]([C@@H]([C@H]4N3C4)O)OC(=O)C)/C(=O)N/C(=C\O)/C(=O)C)[C@@]5(CO5)C)OC
Refernces

Synthetic studies on carzinophilin A. Synthesis of the optically active C.1-C.18 segment

10.1016/S0040-4039(00)86396-0

The research aims to synthesize the optically active C.1-C.18 segment of Carzinophilin A (CZ), a natural intercalative bisalkylator with notable antitumor antibiotic activity. The purpose of this study is to develop a synthetic route for this segment to further investigate the chemical and physiological properties of Carzinophilin A and its related compounds. The synthesis involves multiple steps, including condensation, cyclization, oxidation, and hydrogenation processes. The study successfully synthesized the key intermediate compound 2, which is equivalent to the C.1-C.18 segment of Carzinophilin A, and confirmed its structure through spectroscopic data. The work concludes with the completion of the C.1-C.18 segment synthesis, and the authors are progressing towards the synthesis of the C.19-C.25 segment.

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