Mycinomycin V

Base Information

• Chemical Name: Mycinomycin V
• CAS No.: 73684-72-7
• Molecular Formula: C37H61NO12
• Molecular Weight: 711.891

Synonyms:Mycinomycin V;Antibiotic A 11725 IIa;BRN 4632239;12,13-Deepoxy-12,13-didehydro-14-hydroxymycinamicin I;Mycinamicin I, 12,13-deepoxy-12,13-didehydro-14-hydroxy-;73684-72-7;LS-93759

Chemical Property of Mycinomycin V

Chemical Property:

• Vapor Pressure: 7.64E-32mmHg at 25°C
• Boiling Point: 828.5°Cat760mmHg
• Flash Point: 454.9°C
• PSA: 162.68000
• Density: 1.19g/cm³
• LogP: 2.55250
• XLogP3: 3
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 13
• Rotatable Bond Count: 9
• Exact Mass: 711.41937638
• Heavy Atom Count: 50
• Complexity: 1180

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1C(C=CC=CC(=O)C(CC(C(C(C=CC(=O)O1)C)OC2C(C(CC(O2)C)N(C)C)O)C)C)(COC3C(C(C(C(O3)C)O)OC)OC)O
• Isomeric SMILES: CCC1C(/C=C\C=C\C(=O)C(CC(C(C(/C=C/C(=O)O1)C)OC2C(C(CC(O2)C)N(C)C)O)C)C)(COC3C(C(C(C(O3)C)O)OC)OC)O

Technology Process of Mycinomycin V

There total 1 articles about Mycinomycin V 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:

Reference yield: 18.5%

mycinamicin-IV → C36H59NO11 + mycinamicin-I (73665-15-3) + mycinamicin-III (73684-71-6) + mycinamicin V (73684-72-7) + mycinamicin II (73684-69-2)

Guidance literature:

With multifunctional biosynthetic P₄₅₀ monooxygenase; rhodococcus reductase domain; NADPH; In aq. buffer; at 28 ℃; for 2h; pH=7.3; Reagent/catalyst; Kinetics; Enzymatic reaction;

DOI:10.1021/ja4130302

Reference yield:

mycinamicin V (73684-72-7) → mycinamicin II (73684-69-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 39 percent / MCPBA, disodium hydrogen phosphate / CH₂Cl₂ / 23 h / 60 °C

2: 56 percent / triphenylphosphine / CH₂Cl₂ / 67 h / 55 °C

With disodium hydrogenphosphate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In dichloromethane;

DOI:10.1039/P19890000787

Downstream raw materials:

mycinamicin II

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