Flurithromycin

Base Information Edit

Chemical Name:Flurithromycin
CAS No.:82664-20-8
Molecular Formula:C37H66FNO13
Molecular Weight:751.928
Hs Code.:
European Community (EC) Number:617-374-1
UNII:56C9DTE69V
DSSTox Substance ID:DTXSID40905085
Nikkaji Number:J23.282C
Wikipedia:Flurithromycin
Wikidata:Q5462893
NCI Thesaurus Code:C65735
Metabolomics Workbench ID:144438
ChEMBL ID:CHEMBL2106403
Mol file:82664-20-8.mol

Synonyms:8-fluoroerythromycin A;antibiotic P 80206;antibiotic P-80206;flurithromycin;flurythromycin;flurythromycin A;P 0501A;P-0501A

Suppliers and Price of Flurithromycin

Supply Marketing:Edit

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

American Custom Chemicals Corporation
FLURITHROMYCIN 95.00%
10MG
$ 550.00

American Custom Chemicals Corporation
FLURITHROMYCIN 95.00%
25MG
$ 700.00

American Custom Chemicals Corporation
FLURITHROMYCIN 95.00%
100MG
$ 1600.00

TRC
8-FluoroErythromycin
10mg
$ 185.00

Usbiological
8-Fluoro Erythromycin
10mg
$ 460.00

Usbiological
8-Fluoro erythromycin
5mg
$ 460.00

Total 13 raw suppliers

Chemical Property of Flurithromycin Edit

Chemical Property:

Vapor Pressure:9.85E-31mmHg at 25°C
Melting Point:>139°C (dec.)
Boiling Point:814.6°C at 760 mmHg
PKA:12.94±0.70(Predicted)
Flash Point:446.5°C
PSA：193.91000
Density:1.22g/cm³
LogP:1.87770
Storage Temp.:-20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
XLogP3:2.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:15
Rotatable Bond Count:7
Exact Mass:751.45181932
Heavy Atom Count:52
Complexity:1230

Purity/Quality:

95-99% ^*data from raw suppliers

FLURITHROMYCIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): F
Hazard Codes:F
Statements: 10
Safety Statements: 16

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)(C)F)C)O)(C)O
Isomeric SMILES:CC[C@@H]1[C@@]([C@@H]([C@H](C(=O)[C@@](C[C@@]([C@@H]([C@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]2C[C@@]([C@H]([C@@H](O2)C)O)(C)OC)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)O)(C)F)C)O)(C)O
Uses A fluorinated derivative of Erythromycin (E649950). A macrolide antibiotic.

Technology Process of Flurithromycin

There total 5 articles about Flurithromycin 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: 74.0%