CAS 581076-72-4
:(2R)-2-acetamido-3-(3,4-dimethylphenyl)sulfanyl-propanoic acid
Description:
(2R)-2-acetamido-3-(3,4-dimethylphenyl)sulfanyl-propanoic acid, with CAS number 581076-72-4, is an organic compound characterized by its unique structural features. It contains an acetamido group, which contributes to its solubility and reactivity, and a sulfanyl (thioether) functional group that enhances its chemical properties, potentially influencing its biological activity. The presence of the 3,4-dimethylphenyl moiety indicates that the compound has aromatic characteristics, which can affect its interactions with biological targets. The propanoic acid backbone suggests that it may exhibit acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. This compound may be of interest in medicinal chemistry due to its potential pharmacological applications, particularly in the development of therapeutics targeting specific biological pathways. Its stereochemistry, indicated by the (2R) configuration, suggests that it may exhibit chirality, which can significantly influence its biological activity and interactions with enzymes or receptors. Overall, this compound represents a complex structure with potential implications in both synthetic and medicinal chemistry.
Formula:C13H17NO3S
InChI:InChI=1/C13H17NO3S/c1-8-4-5-11(6-9(8)2)18-7-12(13(16)17)14-10(3)15/h4-6,12H,7H2,1-3H3,(H,14,15)(H,16,17)/t12-/m0/s1
SMILES:Cc1ccc(cc1C)SC[C@@H](C(=O)O)N=C(C)O
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Found 2 products.
N-Acetyl-S-(3,4-dimethylbenzene)-L-cysteine
CAS:Formula:C13H17NO3SPurity:≥ 97.0%Color and Shape:Off-white to light brown solidMolecular weight:267.34N-Acetyl-S-(3,4-dimethylbenzene)-L-cysteine
CAS:Controlled Product<p>Applications N-Acetyl-S-(3,4-dimethylbenzene)-L-cysteine (cas# 581076-72-4) is a compound useful in organic synthesis.<br>References Gonzalez-Reche, L., et al.: Arch. Toxicol., 77, 80 (2003),<br></p>Formula:C13H17NO3SColor and Shape:NeatMolecular weight:267.34

