(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide-d5
| Product Name | (E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide-d5 |
|---|---|
| CAT No. | CS-T-89369 |
| CAS No. | 1104483-92-2 |
| Category | Stable Isotopes |
| Stock | Enquire |
| Mol. Wt. | Not Available |
| Mol. For. | Not Available |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Smileys | O=C(N(C1=CC=CC(C(/C=C/N(C)C)=O)=C1)C([2H])([2H])C)C([2H])([2H])[2H] |
| Canonical Smiles | CCN(C1=CC=CC(=C1)C(=O)C=CN(C)C)C(=O)C |
| InchIKey | UXWJJVRASIHSQS-CZIVGBDRSA-N |
| Inchl | InChI=1S/C15H20N2O2/c1-5-17(12(2)18)14-8-6-7-13(11-14)15(19)9-10-16(3)4/h6-11H,5H2,1-4H3/b10-9+/i1D3,5D2 |
| IUPAC | N-[3-[(E)-3-(dimethylamino)prop-2-enoyl]phenyl]-N-(1,1,2,2,2-pentadeuterioethyl)acetamide |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide-d5 is a deuterated form of the compound (E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide. This compound is commonly used in biomedical research for its ability to act as a fluorescent probe for a variety of biological systems. Its fluorescent properties make it an ideal tool for studying protein-protein interactions, enzyme activity, and cellular signaling pathways.
The chemical formula of (E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide-d5 is C16H17D5N2O2, and its molecular weight is 280.39 g/mol. The compound's chemical structure includes a dimethylamino group, a phenyl ring, and an acryloyl group, which are responsible for its fluorescence properties.
The compound's fluorescence is due to its ability to undergo a photochemical reaction, known as a photoisomerization, when exposed to light. This reaction involves the transfer of an electron from the dimethylamino group to the acryloyl group, resulting in a change in the molecule's shape and the emission of light.
(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-ethylacetamide-d5 is a valuable tool for studying biological systems due to its ability to selectively bind to specific proteins and enzymes. Its deuterated form allows for more precise analysis using techniques such as nuclear magnetic resonance (NMR) spectroscopy, making it an important resource for studying protein structures and interactions.
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