1215006-08-8 Usage
Description
(S)-5-((Tert-butylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one is a chemical compound belonging to the oxazolidinone class of antibiotics. It is characterized by the presence of a morpholine group, a fluoro-substituted phenyl ring, and a tert-butylamino methyl group, which may contribute to its enhanced antibacterial activity and overall pharmacokinetic properties. (S)-5-((Tert-butylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one holds potential for pharmaceutical applications, particularly in the treatment of bacterial infections.
Uses
Used in Pharmaceutical Industry:
(S)-5-((Tert-butylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one is used as an antibiotic for the treatment of bacterial infections. Its unique structure, including the morpholine group and fluoro-substituted phenyl ring, may enhance its antibacterial activity against various bacterial strains.
Used in Research and Development:
In the field of pharmaceutical research and development, (S)-5-((Tert-butylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one serves as a valuable compound for studying the mechanisms of action and potential applications of oxazolidinone-class antibiotics. Its structure and properties can provide insights into the design and development of new antibiotics with improved efficacy and reduced resistance.
Used in Drug Resistance Studies:
(S)-5-((Tert-butylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one can be utilized in studies aimed at understanding and combating antibiotic resistance. Its unique structural features may offer new avenues for the development of antibiotics that can overcome existing resistance mechanisms in bacteria.
Used in Drug Delivery Systems:
Similar to gallotannin, (S)-5-((Tert-butylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one may benefit from novel drug delivery systems to enhance its bioavailability, delivery, and therapeutic outcomes. The development of such systems could improve the compound's effectiveness in treating bacterial infections and reduce the likelihood of resistance development.
Check Digit Verification of cas no
The CAS Registry Mumber 1215006-08-8 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, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1215006-08:
(9*1)+(8*2)+(7*1)+(6*5)+(5*0)+(4*0)+(3*6)+(2*0)+(1*8)=88
88 % 10 = 8
So 1215006-08-8 is a valid CAS Registry Number.
1215006-08-8Relevant articles and documents
Process for the preparation of an oxazolidinone antibacterial agent and intermediates thereof
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Page/Page column 8, (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.
