5beta-Bufa-20,22-dienolide, 14,15beta-epoxy-3beta,5-dihydroxy-, 3-acetate

Base Information

• Chemical Name: 5beta-Bufa-20,22-dienolide, 14,15beta-epoxy-3beta,5-dihydroxy-, 3-acetate
• CAS No.: 4029-68-9
• Molecular Formula: C26H34O6
• Molecular Weight: 442.5446
• NSC Number: 135687
• DSSTox Substance ID: DTXSID30960724
• Mol file: 4029-68-9.mol

Synonyms:Acetylmarinobufogenin;Acetylmarinobufagin;4029-68-9;Marinobufagin, 3-acetyl-;3-(acetyloxy)-5-hydroxy-14,15-epoxybufa-20,22-dienolide;Neuro_000067;DTXSID30960724;SMEFDRPJDZWFRJ-UHFFFAOYSA-N;NSC135687;NSC-135687;5.beta.-Bufa-20,22-dienolide, 14,15.beta.-epoxy-3.beta.,5-dihydroxy-, 3-acetate;Bufa-20,22-dienolide, 3-(acetyloxy)-14,15-epoxy-5-hydroxy-, (3.beta.,5.beta.,15.beta.)-;NCI60_000796;5.beta.-Bufa-20, 14,15.beta.-epoxy-3.beta.,5-dihydroxy-, 3-acetate;3-.beta.,5-Dihydroxy-14,15-.beta.-epoxy-5-.beta.-bufa-20,22-dienolide 3-acetate;5-.beta.-Bufa-20,22-dienolide, 3-.beta.,5-dihydroxy-14,15-.beta.-epoxy-, 3-acetate;Bufa-20, 3-(acetyloxy)-14,15-epoxy-5-hydroxy-, (3.beta.,5.beta.,15.beta.)-;5a-Hydroxy-9a,11a-dimethyl-1-(2-oxo-2H-pyran-5-yl)hexadecahydronaphtho[1',2':6,7]indeno[1,7a-b]oxiren-7-yl acetate #

Chemical Property of 5beta-Bufa-20,22-dienolide, 14,15beta-epoxy-3beta,5-dihydroxy-, 3-acetate

Chemical Property:

• Vapor Pressure: 4.48E-16mmHg at 25°C
• Boiling Point: 584.1°Cat760mmHg
• Flash Point: 195°C
• PSA: 89.27000
• Density: 1.29g/cm³
• LogP: 3.94400
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 442.23553880
• Heavy Atom Count: 32
• Complexity: 939

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1CCC2(C3CCC4(C(CC5C4(C3CCC2(C1)O)O5)C6=COC(=O)C=C6)C)C

Technology Process of 5beta-Bufa-20,22-dienolide, 14,15beta-epoxy-3beta,5-dihydroxy-, 3-acetate

There total 4 articles about 5beta-Bufa-20,22-dienolide, 14,15beta-epoxy-3beta,5-dihydroxy-, 3-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:

→ marinobufagin acetate (4029-68-9)

Guidance literature:

With acetic anhydride;

Reference yield:

→ Marinobufagin-3β-acetat (4029-68-9,51921-24-5)

Guidance literature:

Acetat (3b) 1) N-Iodsuccinimid (-> Iodhydrin (4a)) 2) Pyridin;

DOI:10.1021/jo00934a012

Reference yield:

→ 14α,15α-epi-Marinobufagin-acetat (4029-68-9,51921-24-5)

Guidance literature:

Acetat 3b, m-Chlorperbenzoesaeure;

DOI:10.1021/jo00934a012