CAS 66521-38-8
:N-[1,1,2,2-tetradeuterio-2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide
Description:
N-[1,1,2,2-tetradeuterio-2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide, with CAS number 66521-38-8, is a deuterated derivative of a compound related to indole and acetamide. This substance features a tetradeuterated ethyl group, which means that it contains four deuterium atoms, enhancing its stability and altering its physical properties compared to its non-deuterated counterpart. The presence of the methoxy group on the indole ring contributes to its potential biological activity, as indole derivatives are often studied for their pharmacological properties. The acetamide functional group suggests that this compound may exhibit characteristics typical of amides, such as hydrogen bonding capabilities, which can influence its solubility and reactivity. Deuterated compounds are frequently used in NMR spectroscopy and other analytical techniques due to their unique spectral signatures. Overall, this compound may be of interest in medicinal chemistry and research applications, particularly in studies involving isotopic labeling and drug development.
Formula:C13H12D4N2O2
InChI:InChI=1/C13H16N2O2/c1-9(16)14-6-5-10-8-15-13-4-3-11(17-2)7-12(10)13/h3-4,7-8,15H,5-6H2,1-2H3,(H,14,16)/i5D2,6D2
SMILES:CC(=NC(C(c1c[nH]c2ccc(cc12)OC)([2H])[2H])([2H])[2H])O
Synonyms:- acetamide, N-[2-(5-methoxy-1H-indol-3-yl)ethyl-1,1,2,2-d4
- N-[2-(5-Methoxy-1H-indol-3-yl)(2
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Found 5 products.
N-Acetyl-5-methoxytryptamine-α,α,β,β-d4
CAS:Purity:98 atom % DColor and Shape:White SolidMolecular weight:236.31Melatonin-d4
CAS:Melatonin D5, a deuterium-labeled version of melatonin, is a hormone produced by the pineal gland, known for its role as a selective ATF-6 inhibitor that promotes apoptosis in human hepatoma cells via COX-2 downregulation. Additionally, it activates melatonin receptors and exhibits antioxidative and anti-inflammatory properties.Formula:C13H16N2O2Purity:98%Color and Shape:SolidMolecular weight:236.3Melatonin-d4
CAS:Controlled Product<p>Applications Hormone; mediates photoperiodicity in mammals; inhibits cerebellar nitric oxide synthetase; peroxynitrite scavenger. Melatonin has complex effects on apoptotic pathways, inhibiting apoptosis in immune cells and neurons but enhancing apoptotic cell death of cancer cells. Inhibits proliferation/metastasis of breast cancer cells by inhibiting estrogen receptor action.<br>References Barchas, et al.: Nature, 214, 919 (1967), Glass, J.D., et al.: Science, 214, 821 (1981),<br></p>Formula:C132H4H12N2O2Color and Shape:Off-White To BeigeMolecular weight:236.30N-ACETYL-5-METHOXYTRYPTAMINE-α,α,β,β-D4
CAS:Formula:C13H12D4N2O2Purity:95.87%Color and Shape:SolidMolecular weight:236.3030




