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Desacetyl-N,O-descarbonyl Linezolid is an impurity derived from Linezolid (L466500), an oxazolidinone antimicrobial agent. It plays a significant role in the pharmaceutical industry due to its association with the inhibition of bacterial mRNA translation.

333753-72-3

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333753-72-3 Usage

Uses

Used in Pharmaceutical Industry:
Desacetyl-N,O-descarbonyl Linezolid is used as an impurity in the development and production of Linezolid, an oxazolidinone antimicrobial. Its presence is crucial for understanding the overall efficacy and safety profile of Linezolid, as it may contribute to potential side effects or interactions with other compounds. By studying and controlling the levels of this impurity, researchers can optimize the therapeutic benefits and minimize adverse effects of Linezolid in treating bacterial infections.

Check Digit Verification of cas no

The CAS Registry Mumber 333753-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,7,5 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 333753-72:
(8*3)+(7*3)+(6*3)+(5*7)+(4*5)+(3*3)+(2*7)+(1*2)=143
143 % 10 = 3
So 333753-72-3 is a valid CAS Registry Number.

333753-72-3Downstream Products

333753-72-3Relevant academic research and scientific papers

Linezolid related substance, and preparation method and application thereof

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Paragraph 0081-0097, (2020/09/12)

The invention belongs to the technical field of medicine synthesis, and discloses a linezolid related substance, and a preparation method and application thereof. The related substance is a compound Iwith a chemical formula of C17H24FN3O4, and the prepara

A oxazolidinone compounds of preparation method

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Paragraph 0023; 0024; 0025; 0026; 0034; 0035; 0036, (2017/08/25)

The invention discloses a method for preparing an oxazolidinone compound. The method comprises the following steps of carrying out ammonolysis reaction on a racemic or optically active 3-chloro-2-hydroxypropyl aniline compound (2) as a starting material and ammonia in a proper solvent and under alkaline condition to obtain a 3-amino-2-hydroxypropyl aniline compound (3); carrying out acylation reaction on the compound (3) to obtain 3-acylamino-2-hydroxypropyl aniline compound (4); and carrying out cyclization reaction on the compound (4) and a corresponding acylating reagent to obtain the racemic or optically active oxazolidinone compound (II) as shown in the description, wherein R1 represents morpholinyl or 3-oxo-4-morpholinyl; R2 represents H or F; and R3 represents C1-12 alkyl, 5-chloro-thiophen-2-yl, thiophen-2-yl or 4,5-dichloro-2-yl; and the compound is a racemate and (S)- or (R)- optical isomers.

Preparing method for linezolid and intermediate thereof

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, (2016/11/02)

The invention relates to a preparing method for linezolid and an intermediate thereof. The preparing method includes the step that 4-chloracetyl acetate compound (I) serves as a starting raw material and is subjected to asymmetric chiral reduction, acetylation, condensation, ammonolysis, Hoffman degradation, acetylation and cyclization to obtain (S)-N-[[3-[3-fluoro-4-(4-morpholinyl) phenyl]-2-oxo-5-oxazolidinyl] methyl] acetamide (linezolid). Compared with other linezolid synthesis methods, the preparing method is high in total yield and product purity, raw materials are cheap and easy to obtain, flammable, combustible and poisonous reagents are avoided, and the production technology is safe and environmentally friendly.

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