3-(Dimethylamino)-1-(pyridin-2-yl)prop-2-en-1-one
97%
- Product Code: 37205
CAS:
66521-54-8
| Molecular Weight: | 176.2200 g./mol | Molecular Formula: | C₁₀H₁₂N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00115039 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various heterocyclic compounds. Its structure, featuring both a pyridine ring and a dimethylamino group, makes it suitable for constructing complex molecules in pharmaceutical research and development. It is particularly valuable in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Additionally, it serves as a key building block in the development of dyes and pigments due to its ability to form conjugated systems, enhancing color properties. Its reactivity with electrophiles and nucleophiles also makes it useful in the creation of ligands for coordination chemistry and catalysis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €14.72 |
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3-(Dimethylamino)-1-(pyridin-2-yl)prop-2-en-1-one
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various heterocyclic compounds. Its structure, featuring both a pyridine ring and a dimethylamino group, makes it suitable for constructing complex molecules in pharmaceutical research and development. It is particularly valuable in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Additionally, it serves as a key building block in the development of dyes and pigments due to its ability to form conjugated systems, enhancing color properties. Its reactivity with electrophiles and nucleophiles also makes it useful in the creation of ligands for coordination chemistry and catalysis.
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