3-(3-Pyridinyl)-1-(4-pyridinyl)-2-propene-1-one-d4

Product Name 3-(3-Pyridinyl)-1-(4-pyridinyl)-2-propene-1-one-d4
CAT No. CS-T-86115
CAS No. 1185239-44-4
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(C1=CC=NC=C1)/C=C/C2=C([2H])N=C([2H])C([2H])=C2[2H]
Canonical Smiles C1=CC(=CN=C1)C=CC(=O)C2=CC=NC=C2
InchIKey UOWGYMNWMDNSTL-GWHRRPHYSA-N
Inchl InChI=1S/C13H10N2O/c16-13(12-5-8-14-9-6-12)4-3-11-2-1-7-15-10-11/h1-10H/b4-3+/i1D,2D,7D,10D
IUPAC (E)-1-pyridin-4-yl-3-(2,4,5,6-tetradeuteriopyridin-3-yl)prop-2-en-1-one
Controlled No
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3-(3-Pyridinyl)-1-(4-pyridinyl)-2-propene-1-one-d4 is a deuterated form of a compound that is commonly used as a research tool in organic chemistry. This compound is often referred to as a Michael acceptor and is used in a wide variety of chemical reactions due to its unique chemical properties. The compound is a pale yellow powder that is soluble in common organic solvents such as ethanol, acetone, and methanol. It has a molecular weight of 214.29 g/mol and a melting point of 125-128°C. The deuterated form of the compound is used to study the mechanism of chemical reactions involving this compound, as deuterium substitution can provide valuable information about the reaction pathway and intermediates. The compound is known to undergo Michael addition reactions, which involve the addition of a nucleophile to the double bond of the molecule. These reactions are commonly used in organic chemistry for the synthesis of a variety of compounds, including pharmaceuticals and natural products. The compound is also known to undergo other types of reactions, such as oxidation and reduction, which can be used to modify its chemical properties. In conclusion, 3-(3-Pyridinyl)-1-(4-pyridinyl)-2-propene-1-one-d4 is a valuable research tool in organic chemistry due to its unique chemical properties and its ability to undergo a variety of reactions. Its deuterated form is particularly useful in studying reaction mechanisms and intermediates.

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