Linezolid
168828-82-8
White to off-white powder
Loss on drying ≤ 0.5%
Purity ≥ 98.0%, total impurities ≤ 2.0%
Chiral isomers ≤ 0.15%
Content 98.0-102.0%
Availability: | |
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Product Description
We are a pharmaceutical intermediate manufacturer of (5R)-3-(3-Fluoro-4-(4-morpholinyl)phenyl)-5-hydroxymethyl-2-oxazolidione.
Its CAS No. is 168828-82-8
Our pharmaceutical intermediates can be used in a variety of APIs such as Articaine, Pyrantel, Bicalutamide, etc.
Product Category | Linezolid |
CAS NO | 168828-82-8 |
Product Specifications | White to off-white powder Loss on drying ≤ 0.5% Purity ≥ 98.0%, total impurities ≤ 2.0% Chiral isomers ≤ 0.15% Content 98.0-102.0% |
168828-82-8 (5R)-3-(3-FLUORO-4-(4-MORPHOLINYL)PHENYL)-5-HYDROXYMETHYL-2-OXAZOLIDIONE.pdf
Office Environment
Laboratory
Workshop/Warehouse
Certificate
(5R)-3-(3-Fluoro-4-(4-morpholinyl)phenyl)-5-hydroxymethyl-2-oxazolidione is produced by EASTFINE , and we are in charge of overseas selling . Not just trading compamy .
China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.
yes , you can have 1 (5R)-3-(3-Fluoro-4-(4-morpholinyl)phenyl)-5-hydroxymethyl-2-oxazolidione sample for starting the business , but it is not free
please contact sale team for detail .
The molecular formula of this compound is typically C16H18FN1O4, indicating 16 carbon atoms, 18 hydrogen atoms, 1 fluorine atom, 1 nitrogen atom, and 4 oxygen atoms.
Medicinal Chemistry: The compound's structure suggests potential activity in drug discovery, particularly as a scaffold for designing molecules that can interact with specific biological targets, such as receptors or enzymes.
Antibacterial or Antiviral Agents: Given the oxazolidinone core, compounds like this are sometimes explored for their potential as antibiotics or antimicrobial agents.
Neuroactive Compounds: The presence of the morpholine and hydroxymethyl groups may impart pharmacological properties useful in neurochemistry or CNS-related research.
Synthetic Chemistry: It could also serve as an intermediate for the synthesis of more complex molecules.
Fluorine Substitution: The presence of the fluorine atom can affect the compound’s lipophilicity, metabolic stability, and receptor binding affinity, often enhancing biological activity.
Morpholine Group: Morpholine rings are common in bioactive compounds and may influence water solubility and molecular interaction with biological systems.
Hydroxymethyl Group: This group could play a role in enhancing the compound’s interaction with specific biological targets or might be used for further chemical modifications in synthetic processes.
The synthesis of this compound could involve:
Fluorination: To introduce the fluorine atom at the 3-position of the phenyl ring.
Morpholine Substitution: Introducing the morpholine group at the 4-position of the phenyl ring, possibly via nucleophilic substitution.
Oxazolidinone Formation: The oxazolidinone ring can be synthesized using standard organic reactions like cyclization of appropriate precursors.
Hydroxymethylation: The addition of the hydroxymethyl group at the 5-position may be done using a suitable hydroxymethylating agent.
Personal Protective Equipment (PPE): Wear gloves, goggles, and a lab coat.
Proper Ventilation: Work in a fume hood to avoid inhalation of fumes or dust.
Chemical Disposal: Follow proper chemical disposal procedures according to local regulations.
MSDS: Refer to the Material Safety Data Sheet (MSDS) for specific safety instructions, as the toxicity profile of this compound may not be well-documented in public resources.