1215006-11-3 Usage
Uses
Used in Pharmaceutical Industry:
N-Tert-butyl-N-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methyl)acetamide is used as a potential candidate for the development of new antimicrobial drugs. Its structural features and functional groups, particularly the oxazolidinone ring and the fluorinated morpholinophenyl group, suggest that it could have broad-spectrum antimicrobial activity, making it a valuable asset in the fight against resistant bacterial strains.
Further research and development are necessary to explore the full potential of N-Tert-butyl-N-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methyl)acetamide in medicinal chemistry, including its efficacy, safety, and mechanism of action. N-Tert-butyl-N-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methyl)acetamide's unique structural elements may also lead to the discovery of novel applications beyond traditional antimicrobial uses, depending on the outcomes of ongoing studies.
Check Digit Verification of cas no
The CAS Registry Mumber 1215006-11-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,5,0,0 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1215006-11:
(9*1)+(8*2)+(7*1)+(6*5)+(5*0)+(4*0)+(3*6)+(2*1)+(1*1)=83
83 % 10 = 3
So 1215006-11-3 is a valid CAS Registry Number.
1215006-11-3Relevant academic research and scientific papers
Process for the preparation of an oxazolidinone antibacterial agent and intermediates thereof
-
Page/Page column 9; 10, (2010/04/24)
Comprising a preparation process of linezolid from a compound of formula (IV) where R1 is selected from a (C4-C10)-alkyl radical which is attached to the N atom by a tertiary C atom, and a straight or branched (C3-C10)-alkenyl radical attached to the N atom such that the C=C double bond is separated from the N atom by a methylene group. Compound (IV) is submitted either first to an acetylation reaction and then to a dealkylation reaction or, alternatively, first to a dealkylation reaction and then to an acetylation reaction to yield linezolid. It also comprises new intermediate compounds useful in such a preparation process, which are obtained with high yields and high chemical and optical purity, and which are processed easily to linezolid.
