
CAS 1346616-95-2
:N-Acetyl-S-(trichlorovinyl)-L-cysteine-d3
Description:
N-Acetyl-S-(trichlorovinyl)-L-cysteine-d3 is a synthetic compound that belongs to the class of cysteine derivatives. It features a trichlorovinyl group, which contributes to its reactivity and potential applications in biochemical research. The presence of the N-acetyl group enhances its solubility and stability, making it suitable for various laboratory settings. The "d3" designation indicates that this compound is a deuterated form, meaning it contains three deuterium atoms, which can be useful in nuclear magnetic resonance (NMR) spectroscopy and other analytical techniques to trace metabolic pathways or interactions in biological systems. This compound may be of interest in studies related to cysteine metabolism, protein modification, or as a potential therapeutic agent due to its unique structural characteristics. However, specific safety and handling guidelines should be followed, as the trichlorovinyl moiety can pose hazards associated with chlorinated compounds. Always consult material safety data sheets (MSDS) and relevant literature for detailed information on handling and potential applications.
Formula:C7H8Cl3NO3S
Synonyms:- N-(Acetyl-d3)-S-(1,2,2-trichloroethenyl)-L-cysteine
- N-Acetyl-S-(trichlorovinyl)-L-cysteine-d3
- N-Ac-TCVC-d3
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N-Acetyl-S-(trichlorovinyl)-L-cysteine-d3
CAS:Controlled Product<p>Applications A novel labelled metabolite of Perchloroethene (PER) in humans after inhalation. It is an important biomarker for the glutathione dependent biotransformation of PER.<br>References Urban, G., et al.: Xenobiotica, 24, 881 (1994), Birner, G., et al.: Drug Metab. Dispos., 24, 41 (1996), Dekant, W., et al.: Drug Metab. Dispos., 15, 702 (1987),<br></p>Formula:C7H5D3Cl3NO3SColor and Shape:NeatMolecular weight:295.59
