Rifamycin B dipropylamide

Base Information

Chemical Name:Rifamycin B dipropylamide
CAS No.:16784-03-5
Molecular Formula:C₄₅H₆₂N₂O₁₃
Molecular Weight:838.993
Hs Code.:

Synonyms:Rifamycin B dipropylamide;BRN 5418497;16784-03-5;NCI 143-425;4-O-[2-(Dipropylamino)-2-oxoethyl]rifamycin;Rifamycin, 4-O-(2-(dipropylamino)-2-oxoethyl)-;[(9E,19E,21E)-27-[2-[di(propan-2-yl)amino]-2-oxoethoxy]-2,15,17,29-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23-dioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(29),2,4,9,19,21,25,27-octaen-13-yl] acetate;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,N-dipropyl-, 21-acetate;LS-9232

Suppliers and Price of Rifamycin B dipropylamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of Rifamycin B dipropylamide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:932.5°Cat760mmHg
Flash Point:517.7°C
PSA：214.11000
Density:1.28g/cm³
LogP:6.15780
XLogP3:6.4
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:13
Rotatable Bond Count:8
Exact Mass:838.42519004
Heavy Atom Count:60
Complexity:1610

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C=CC=C(C(=O)NC2=CC(=C3C(=C2O)C(=C(C4=C3C(=O)C(O4)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C)O)OCC(=O)N(C(C)C)C(C)C)C
Isomeric SMILES:CC1/C=C/C=C(/C(=O)NC2=CC(=C3C(=C2O)C(=C(C4=C3C(=O)C(O4)(O/C=C/C(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C)O)OCC(=O)N(C(C)C)C(C)C)\C

Technology Process of Rifamycin B dipropylamide

There total 1 articles about Rifamycin B dipropylamide 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: