(E)-Penta-2,4-dienoic acid
97%, mix-50%Z
- Product Code: 78461
CAS:
21651-12-7
| Molecular Weight: | 98.10 g./mol | Molecular Formula: | C₅H₆O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00014017 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas, dark |
Product Description:
(E)-Penta-2,4-dienoic acid is primarily utilized in organic synthesis and chemical research. It serves as a valuable building block for the preparation of various complex organic compounds, including pharmaceuticals and agrochemicals. Its conjugated diene structure makes it a useful intermediate in Diels-Alder reactions, which are pivotal in constructing cyclic organic molecules. Additionally, it is employed in the study of reaction mechanisms and polymerization processes, contributing to advancements in material science. Its applications also extend to the development of bioactive molecules and natural product synthesis, where its unique reactivity is leveraged to create structurally diverse compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Pale yellow Solid |
| Puritymixture of cis and trans | 96.5 % 100 % |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,700.00 |
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| 1.000 | 10-20 days | ฿7,290.00 |
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| 5.000 | 10-20 days | ฿25,479.00 |
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(E)-Penta-2,4-dienoic acid
(E)-Penta-2,4-dienoic acid is primarily utilized in organic synthesis and chemical research. It serves as a valuable building block for the preparation of various complex organic compounds, including pharmaceuticals and agrochemicals. Its conjugated diene structure makes it a useful intermediate in Diels-Alder reactions, which are pivotal in constructing cyclic organic molecules. Additionally, it is employed in the study of reaction mechanisms and polymerization processes, contributing to advancements in material science. Its applications also extend to the development of bioactive molecules and natural product synthesis, where its unique reactivity is leveraged to create structurally diverse compounds.
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