Methyl 5-Hexenoate
≥98%(GC)
- Product Code: 84074
CAS:
2396-80-7
| Molecular Weight: | 128.17 g./mol | Molecular Formula: | C₇H₁₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00671538 | |
| Melting Point: | Boiling Point: | 157°C(lit.) | |
| Density: | 0.91 | Storage Condition: | room temperature, dry |
Product Description:
Methyl 5-Hexenoate is primarily used as an intermediate in organic synthesis, particularly in the production of flavors and fragrances. Its unsaturated ester structure makes it valuable for creating complex molecules with fruity or floral notes. It is also employed in polymer chemistry as a monomer or co-monomer for synthesizing specialized polymers with unique properties. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals, where its reactive double bond allows for further functionalization. In research, it is utilized to study reaction mechanisms and develop new synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless - Almost colorless Clear Liquid |
| PURITY | 98-100 |
| SPECIFIC GRAVITY 2020 | 0.9130-0.9150 |
| Infrared spectrum | Conforms to Structure |
| REFRACTIVE INDEX N20D | 1.4200-1.4220 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $51.52 |
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| 1.000 | 10-20 days | $106.97 |
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| 5.000 | 10-20 days | $365.73 |
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Methyl 5-Hexenoate
Methyl 5-Hexenoate is primarily used as an intermediate in organic synthesis, particularly in the production of flavors and fragrances. Its unsaturated ester structure makes it valuable for creating complex molecules with fruity or floral notes. It is also employed in polymer chemistry as a monomer or co-monomer for synthesizing specialized polymers with unique properties. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals, where its reactive double bond allows for further functionalization. In research, it is utilized to study reaction mechanisms and develop new synthetic pathways.
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