3-(Naphthalen-1-yloxy)propanoic acid
≥95%
- Product Code: 86007
CAS:
16563-41-0
| Molecular Weight: | 216.23 g./mol | Molecular Formula: | C₁₃H₁₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00156915 | |
| Melting Point: | Boiling Point: | 379.8°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a naphthalene ring linked to a propanoic acid group, makes it suitable for constructing more complex molecules, particularly those requiring aromatic systems with functionalized side chains. In pharmaceutical research, it is often employed in the development of compounds with potential anti-inflammatory or analgesic properties. Additionally, it finds application in the synthesis of dyes and pigments, leveraging its aromatic nature to impart color and stability to the final products. Its versatility in chemical reactions, such as esterification and amidation, further broadens its utility in industrial and research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,401.00 |
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| 0.250 | 10-20 days | ฿8,802.00 |
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3-(Naphthalen-1-yloxy)propanoic acid
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a naphthalene ring linked to a propanoic acid group, makes it suitable for constructing more complex molecules, particularly those requiring aromatic systems with functionalized side chains. In pharmaceutical research, it is often employed in the development of compounds with potential anti-inflammatory or analgesic properties. Additionally, it finds application in the synthesis of dyes and pigments, leveraging its aromatic nature to impart color and stability to the final products. Its versatility in chemical reactions, such as esterification and amidation, further broadens its utility in industrial and research settings.
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