CAS 96800-41-8
:N-({(5S)-3-[4-(methylsulfinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide
Description:
N-({(5S)-3-[4-(methylsulfinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide, with CAS number 96800-41-8, is a chemical compound characterized by its oxazolidinone structure, which includes a chiral center contributing to its stereochemistry. This compound features a methylsulfinyl group attached to a phenyl ring, indicating potential biological activity, particularly in medicinal chemistry. The presence of the acetamide functional group suggests it may exhibit properties typical of amides, such as hydrogen bonding capabilities, which can influence solubility and reactivity. The oxazolidinone ring contributes to the compound's stability and may play a role in its interaction with biological targets. Overall, this compound's unique structural features may make it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its specific characteristics, including solubility, melting point, and reactivity, would require empirical investigation to fully understand its potential applications and behavior in various chemical environments.
Formula:C13H16N2O4S
InChI:InChI=1/C13H16N2O4S/c1-9(16)14-7-11-8-15(13(17)19-11)10-3-5-12(6-4-10)20(2)18/h3-6,11H,7-8H2,1-2H3,(H,14,16)/t11-,20?/m0/s1
SMILES:CC(=NC[C@H]1CN(c2ccc(cc2)S(=O)C)C(=O)O1)O
Synonyms:- acetamide, N-[[(5S)-3-[4-(methylsulfinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]-
- (S)-N-<<3-<4(S)-(methylsulfinyl)phenyl>-2-oxo-5-oxazolidinyl>methyl>acetamide
- 4-methylsulfinylphenyloxooxazolidinylmethylacetamide
- (5S)-5-Acetylaminomethyl-3-(4-methylsulfinylphenyl)oxazolidin-2-one
- N-[[(5S)-3-[4-(Methylsulfinyl)phenyl]-2-oxooxazolidin-5-yl]methyl]acetamide
- DuP-105
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Found 3 products.
N-[[(5S)-3-(4-Methylsulfinylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
CAS:<p>N-[[(5S)-3-(4-Methylsulfinylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide is a synthetic compound, which is derived from the oxazolidinone class of molecules known for their antimicrobial properties. Its mechanism of action involves the inhibition of bacterial protein synthesis by binding to the 50S subunit of the bacterial ribosome, thereby preventing the formation of a functional 70S initiation complex. This effectively disrupts the growth and replication of susceptible bacterial strains.</p>Formula:C13H16N2O4SPurity:Min. 95%Molecular weight:296.34 g/molDuP 105
CAS:<p>DuP 105 is an oral oxazolidinone, a novel synthetic antimicrobial compound effective against gram-positive bacteria.</p>Formula:C13H16N2O4SPurity:99.82%Color and Shape:SolidMolecular weight:296.34


