BicozaMycin benzoate, FR 2054

Base Information

Chemical Name:BicozaMycin benzoate, FR 2054
CAS No.:37134-40-0
Molecular Formula:C₁₉H₂₂N₂O₈
Molecular Weight:406.392
Hs Code.:
Mol file:37134-40-0.mol

Synonyms:

Suppliers and Price of BicozaMycin benzoate, FR 2054

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

TRC
BicyclomycinBenzoate
1mg
$ 155.00

TRC
BicyclomycinBenzoate
5mg
$ 520.00

DC Chemicals
Bicyclomycinbenzoate >98%
250 mg
$ 1200.00

ChemScene
Bicyclomycinbenzoate 99.85%
100mg
$ 1440.00

ChemScene
Bicyclomycinbenzoate 99.85%
50mg
$ 816.00

ChemScene
Bicyclomycinbenzoate 99.85%
25mg
$ 456.00

ChemScene
Bicyclomycinbenzoate 99.85%
10mg
$ 216.00

ChemScene
Bicyclomycinbenzoate 99.85%
5mg
$ 120.00

Cayman Chemical
Bicyclomycin Benzoate ≥99%
5mg
$ 115.00

Cayman Chemical
Bicyclomycin Benzoate ≥99%
25mg
$ 374.00

Total 7 raw suppliers

Chemical Property of BicozaMycin benzoate, FR 2054

Chemical Property:

Melting Point:>123°C (dec.)
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)

Purity/Quality:

97% ^*data from raw suppliers

BicyclomycinBenzoate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses BicozaMycin benzoate, FR 2054 is a polar metabolite first isolated from Streptomyces sapporonensis in 1972, with activity against Gram negative bacteria. The selective Gram negative profile of bicyclomycin is rare among Streptomyces metabolites, and in an effort to overcome its poor in vivo absorption, the benzoate ester was prepared by reaction with the more exposed primary alcohol. BicozaMycin benzoate, FR 2054 benzoate has limited use as a veterinary antibiotic.

Technology Process of BicozaMycin benzoate, FR 2054

There total 1 articles about BicozaMycin benzoate, FR 2054 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: