Linezolid
168828-81-7
Availability: | |
---|---|
Product Description
We are a pharmaceutical intermediate manufacturer of (3-Fluoro-4-morpholin-4-ylphenyl)carbamic acid benzyl ester.
Its CAS No. is 168828-81-7
Our pharmaceutical intermediates can be used in a variety of APIs such as Articaine, Pyrantel, Bicalutamide, etc.
Product Category | Linezolid |
CAS NO | 168828-81-7 |
Product Specifications |
168828-81-7 (3-FLUORO-4-MORPHOLIN-4-YLPHENYL)CARBAMIC ACID BENZYL ESTER.pdf
Office Environment
Laboratory
Workshop/Warehouse
Certificate
(3-Fluoro-4-morpholin-4-ylphenyl)carbamic acid benzyl ester 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 (3-Fluoro-4-morpholin-4-ylphenyl)carbamic acid benzyl ester sample for starting the business , but it is not free
please contact sale team for detail .
The molecular formula is typically written as C16H18FN1O3, indicating 16 carbon atoms, 18 hydrogen atoms, 1 fluorine atom, 1 nitrogen atom, and 3 oxygen atoms.
Pharmaceutical Research: It may be studied for its potential pharmacological properties. The presence of a morpholine group and fluoro substitution suggests that it could be relevant in the development of drugs targeting various diseases.
Synthetic Chemistry: It could be used in the synthesis of other complex organic molecules.
Biological Testing: This compound may be used in studies to assess its activity against specific targets in biological systems.
A fluoro group at the 3-position of a phenyl ring.
A morpholin-4-yl group attached at the 4-position of the same phenyl ring.
A carbamic acid benzyl ester functional group, where the ester is attached to the nitrogen atom in the carbamic acid.
Handle it with care in a well-ventilated area.
Wear appropriate protective equipment, including gloves, goggles, and lab coat.
Follow proper disposal protocols for chemicals.
Refer to the material safety data sheet (MSDS) for more specific safety guidelines.
The synthesis would likely involve standard organic synthesis techniques such as halogenation, amine substitution, and esterification. The morpholine group may be introduced via a nucleophilic substitution reaction.
The toxicity and side effects of this compound are not well-documented in public resources. However, as it contains a morpholine ring, it may exhibit neurotoxic or irritant properties, and the fluorine atom might increase its potential for bioaccumulation or other pharmacokinetic concerns.