4,4'-Di-N-acetylamino-diphenylsulfoxide-d8

Product Name 4,4'-Di-N-acetylamino-diphenylsulfoxide-d8
CAT No. CS-T-52366
CAS No. 557794-36-2
Category Stable Isotopes
Stock Enquire
Mol. Wt. 324.42 g/mol
Mol. For. C16H8D8N2O3S
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles CC(=O)NC1=CC=C(C=C1)S(=O)C2=CC=C(C=C2)NC(=O)C
InchIKey HABWONZJSRPOIE-UWAUJQNOSA-N
Inchl InChI=1S/C16H16N2O3S/c1-11(19)17-13-3-7-15(8-4-13)22(21)16-9-5-14(6-10-16)18-12(2)20/h3-10H,1-2H3,(H,17,19)(H,18,20)/i3D,4D,5D,6D,7D,8D,9D,10D
IUPAC N-[4-(4-acetamido-2,3,5,6-tetradeuteriophenyl)sulfinyl-2,3,5,6-tetradeuteriophenyl]acetamide
Controlled No
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4,4'-Di-N-acetylamino-diphenylsulfoxide-d8 is a deuterated analogue of the organic compound 4,4'-Di-N-acetylamino-diphenylsulfoxide. It is a highly specialized chemical that is primarily used in nuclear magnetic resonance (NMR) spectroscopy. This compound is an isotopically labeled derivative of the parent compound, which means that it contains eight deuterium atoms instead of eight hydrogen atoms. This labeling makes it easier to distinguish and analyze the compound in complex biological and chemical mixtures. The chemical formula of 4,4'-Di-N-acetylamino-diphenylsulfoxide-d8 is C16H12D8N2O3S, and it has a molecular weight of 358.43 g/mol. The compound has a melting point of 156-158°C and is soluble in polar solvents like methanol, ethanol, and dimethyl sulfoxide. The compound is used in NMR spectroscopy to study the structure, dynamics, and interactions of biological macromolecules and other complex organic compounds. The isotopic labeling of this compound enhances the sensitivity and accuracy of NMR experiments, making it possible to study the behavior of molecules with high precision. Additionally, this compound has also been used in medicinal chemistry research to develop new drugs and treatments for various diseases. In conclusion, 4,4'-Di-N-acetylamino-diphenylsulfoxide-d8 is a highly specialized compound used in NMR spectroscopy to study the structure and behavior of biological macromolecules and other complex organic compounds. Its isotopic labeling enhances the accuracy and sensitivity of NMR experiments, making it an essential tool in the field of chemical and biological research.

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