Rifamycin B ethylpropylamide

Base Information

• Chemical Name: Rifamycin B ethylpropylamide
• CAS No.: 16784-02-4
• Molecular Formula: C44H60 N2 O13
• Molecular Weight: 824.9528
• Mol file: 16784-02-4.mol

Synonyms:Rifamycin B ethylpropylamide;BRN 5418457;NCI 143-430;NSC143430;Rifamycin, 4-O-(2-(ethylpropylamino)-2-oxoethyl)-;16784-02-4;Acetamide, 2-((1,2-dihydro-5,6,17,19,21-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-2,7-(epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)furan-9-yl)oxy)-N-ethyl-N-propyl-, 21-acetate;Rifamycin, 4-O-[2-(ethylpropylamino)-2-oxoethyl]-;[[2-[ethyl(propyl)amino]-2-oxo-ethoxy]-tetrahydroxy-methoxy-heptamethyl-dioxo-[?]yl] acetate;C44H60N2O13;LS-9238;Acetamide, 2-[[(14E)-21-(acetyloxy)-1,2-dihydro-5,6,17,19-tetrahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-2,7-(epoxy[1,11,13]pentadecatrienoimino)naphtho[2,1-b]furan-9-yl]oxy]-N-ethyl-N-propyl-

Chemical Property of Rifamycin B ethylpropylamide

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 933.4°Cat760mmHg
• Flash Point: 518.3°C
• Density: 1.29g/cm³
• XLogP3: 6
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 13
• Rotatable Bond Count: 9
• Exact Mass: 824.40953997
• Heavy Atom Count: 59
• Complexity: 1570

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCN(CC)C(=O)COC1=C2C3=C(C(=C1)NC(=O)C(=CC=CC(C(C(C(C(C(C(C(C=COC4(C(=O)C2=C(O4)C(=C3O)C)C)OC)C)OC(=O)C)C)O)C)O)C)C)O
• Isomeric SMILES: CCCN(CC)C(=O)COC1=C2C3=C(C(=C1)NC(=O)/C(=C/C=C/C(C(C(C(C(C(C(C(/C=C/OC4(C(=O)C2=C(O4)C(=C3O)C)C)OC)C)OC(=O)C)C)O)C)O)C)/C)O

Technology Process of Rifamycin B ethylpropylamide

There total 1 articles about Rifamycin B ethylpropylamide 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:

ethylpropylamine (20193-20-8) + Rifamycin B (13929-35-6) → Rifamycin-B- (16784-02-4)

Guidance literature:

With dicyclohexyl-carbodiimide; In tetrahydrofuran;

DOI:10.1021/jm00335a005

upstream raw materials:

ethylpropylamine

Rifamycin B