CAS 1331909-07-9

N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3

Description:

N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3 is a chemically modified amino acid derivative, specifically a stable isotope-labeled form of L-cysteine. This compound features an N-acetyl group, which enhances its solubility and stability, and a substitution at the sulfur atom with a 2,5-dimethylbenzene moiety, contributing to its unique properties. The presence of deuterium (d3) indicates that three hydrogen atoms in the molecule have been replaced with deuterium isotopes, which can be useful in various analytical techniques, such as mass spectrometry, for tracing and quantifying the compound in biological systems. The compound is likely to exhibit characteristics typical of thiols, including reactivity with electrophiles and potential antioxidant properties. Its structural modifications may influence its biological activity, solubility, and interaction with other biomolecules. Overall, N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3 serves as a valuable tool in biochemical research, particularly in studies involving metabolic pathways and drug development.

Formula: C₁₃H₁₇NO₃S

Synonyms:

• (2R)-3-(2,5-dimethylphenyl)sulfanyl-2-[(2,2,2-trideuterioacetyl)amino]propanoic acid
• 2,5-DPMA-d3
• N-Acetyl-S-(2,5-diMethylphenyl)-L-cysteine-d3
• N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3

N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3

Controlled Product

CAS: 1331909-07-9

Applications N-Acetyl-S-(2,5-dimethylbenzene)-L-cysteine-d3 (cas# 1331909-07-9) is a compound useful in organic synthesis.
References Gonzalez-Reche, L., et al.: Arch. Toxicol., 77, 80 (2003),

Formula: C₁₃H₁₄D₃NO₃S

Color and Shape: Neat

Molecular weight: 270.36

Ref: TR-A173772