Melampodin B acetate

Base Information

• Chemical Name: Melampodin B acetate
• CAS No.: 51212-98-7
• Molecular Formula: C19H20O8
• Molecular Weight: 376.3573
• NSC Number: 302035
• ChEMBL ID: CHEMBL1965706
• Mol file: 51212-98-7.mol

Synonyms:MELAMPODIN B ACETATE;NSC302035;NSC 302035;51212-98-7;6H-4,7-Methenofuro(3,2-c)oxacycloundecin-2,6(3H)-dione, 8-(acetyloxy)-11-((acetyloxy)methyl)-3a,4,8,9,10,12a-hexahydro-3-methylene-;6H-4,7-Methenofuro[3,2-c]oxacycloundecin-2,6(3H)-dione, 8-(acetyloxy)-11-[(acetyloxy)methyl]-3a,4,8,9,10,12a-hexahydro-3-methylene-;CHEMBL1965706;NSC-302035;(acetoxy-methylene-dioxo-[?]yl)methyl acetate

Chemical Property of Melampodin B acetate

Chemical Property:

• Vapor Pressure: 4.15E-15mmHg at 25°C
• Boiling Point: 616°Cat760mmHg
• Flash Point: 270.9°C
• Density: 1.33g/cm³
• XLogP3: 0.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 5
• Exact Mass: 376.11581759
• Heavy Atom Count: 27
• Complexity: 775

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OCC1=CC2C(C3C=C(C(CC1)OC(=O)C)C(=O)O3)C(=C)C(=O)O2
• Isomeric SMILES: CC(=O)OC/C/1=C\C2C(C3C=C(C(CC1)OC(=O)C)C(=O)O3)C(=C)C(=O)O2

Technology Process of Melampodin B acetate

There total 2 articles about Melampodin B 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:

→ Melampodin B acetat (51212-98-7)

Guidance literature:

Verb. 1a u. Acetanhydrid;

DOI:10.1021/jo00912a003

Reference yield:

→ Melampodin B-15-acetat (51212-98-7)

Guidance literature:

Melampodin B, Ac2O/Py.;

DOI:10.1002/oms.1210130606