912552-55-7 Usage
Description
(3-fluoro-4-morpholin-4-yl-phenyl)-(3-oxo-propyl)-carbamic acid benzyl ester is a chemical compound that consists of a benzyl ester of a carbamate derivative. It contains a fluoro-substituted phenyl ring attached to a morpholine ring, as well as a 3-oxo-propyl group. Its unique structure makes it potentially valuable for the development of new drugs and materials with specific properties.
Used in Organic Synthesis:
(3-fluoro-4-morpholin-4-yl-phenyl)-(3-oxo-propyl)-carbamic acid benzyl ester is used as a building block in organic synthesis for the creation of various chemical compounds. Its fluoro-substituted phenyl ring and morpholine ring provide unique reactivity and selectivity in chemical reactions.
Used in Pharmaceutical Research:
(3-fluoro-4-morpholin-4-yl-phenyl)-(3-oxo-propyl)-carbamic acid benzyl ester is used as a starting material in pharmaceutical research for the development of new drugs. Its unique structure and functional groups can be utilized to design and synthesize drug candidates with specific biological activities and therapeutic properties.
Used in Drug Development:
(3-fluoro-4-morpholin-4-yl-phenyl)-(3-oxo-propyl)-carbamic acid benzyl ester is used as a key intermediate in the synthesis of drug candidates. Its unique structure and functional groups can be modified to optimize the pharmacokinetic and pharmacodynamic properties of the resulting drug molecules.
Used in Material Science:
(3-fluoro-4-morpholin-4-yl-phenyl)-(3-oxo-propyl)-carbamic acid benzyl ester is used as a component in the development of new materials with specific properties. Its unique structure and functional groups can be incorporated into polymers, coatings, and other materials to impart desired characteristics such as improved stability, reactivity, or selectivity.
Note: As with any chemical compound, proper handling and safety precautions should be taken when working with (3-fluoro-4-morpholin-4-yl-phenyl)-(3-oxo-propyl)-carbamic acid benzyl ester.
Check Digit Verification of cas no
The CAS Registry Mumber 912552-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,5,5 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 912552-55:
(8*9)+(7*1)+(6*2)+(5*5)+(4*5)+(3*2)+(2*5)+(1*5)=157
157 % 10 = 7
So 912552-55-7 is a valid CAS Registry Number.
912552-55-7Relevant articles and documents
Short and practical enantioselective synthesis of linezolid and eperezolid via proline-catalyzed asymmetric α-aminooxylation
Narina, Srinivasarao V.,Sudalai, Arumugam
, p. 6799 - 6802 (2007/10/03)
An efficient enantioselective synthesis of the antibacterials, linezolid (U-100766), and eperezolid (U-100592) using d-proline-catalyzed asymmetric α-aminooxylation of aldehydes as the key step is described here. This is the first report on the enantioselective synthesis of linezolid and eperezolid using asymmetric catalysis.
