Midecamycin Acetate

Base Information

• Chemical Name: Midecamycin Acetate
• CAS No.: 55881-07-7
• Molecular Formula: C45H71NO17
• Molecular Weight: 898.055
• European Community (EC) Number: 259-879-6
• UNII: 3T48CPS7U2
• ChEMBL ID: CHEMBL1091024
• DSSTox Substance ID: DTXSID60905087
• Metabolomics Workbench ID: 121971
• Wikidata: Q3858659
• Wikipedia: Miocamycin
• Mol file: 55881-07-7.mol

Synonyms:3'',9-Diacetylmydecamycin;9,3''-Di-O-acetylmidecamycin;Acecamycin;Midecamycin acetate;Miocamycin;Miokamycin;Mom;Ponsinomycin;

Chemical Property of Midecamycin Acetate

Chemical Property:

• Appearance/Colour: White or offt-white crystalline powder
• Vapor Pressure: 0mmHg at 25°C
• Melting Point: ~220° (with coloration)
• Refractive Index: 1.524
• Boiling Point: 878.7 °C at 760 mmHg
• PKA: 13.06±0.70(Predicted)
• Flash Point: 485.2 °C
• PSA: 218.19000
• Density: 1.2 g/cm³
• LogP: 3.90900
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 18
• Rotatable Bond Count: 18
• Exact Mass: 897.47219980
• Heavy Atom Count: 63
• Complexity: 1590

Purity/Quality:

99.5% ^*data from raw suppliers

Midecamycin Acetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(=O)OC1CC(=O)OC(CC=CC=CC(C(CC(C(C1OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)OC(=O)CC)(C)OC(=O)C)N(C)C)O)CC=O)C)OC(=O)C)C
• Isomeric SMILES: CCC(=O)O[C@@H]1CC(=O)O[C@@H](C/C=C/C=C/[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]1OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)OC(=O)CC)(C)OC(=O)C)N(C)C)O)CC=O)C)OC(=O)C)C
• Description: Miokamycin (midecamycin acetate) is a macrolide antibiotic useful in the treatment of respiratory tract, dermatological and surgical infections due to grampositive bacteria and mycoplasmas.

Technology Process of Midecamycin Acetate

There total 1 articles about Midecamycin Acetate 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:

→ leucomycin V, 3β,9-diacetate 3,4β-dipropanoate (55881-07-7)

Guidance literature:

aus dem Triacetat, H2O/CH3OH;