Cyclohexylacetic Acid
≥98%
- Product Code: 122887
CAS:
5292-21-7
| Molecular Weight: | 142.2 g./mol | Molecular Formula: | C₈H₁₄O₂ |
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| EC Number: | MDL Number: | MFCD00001518 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Cyclohexylacetic acid is widely used in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key intermediate in the creation of anti-inflammatory and analgesic drugs, contributing to the development of medications that alleviate pain and reduce inflammation. Additionally, it is utilized in the manufacture of fragrances and flavors, where it imparts unique aromatic properties to perfumes and food products. In the field of polymer chemistry, it acts as a building block for creating specialized resins and coatings, enhancing their durability and performance. Its versatility also extends to research laboratories, where it is employed in the study of chemical reactions and the development of new synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | ฿3,450.00 |
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| 100.000 | 10-20 days | ฿13,100.00 |
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Cyclohexylacetic Acid
Cyclohexylacetic acid is widely used in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key intermediate in the creation of anti-inflammatory and analgesic drugs, contributing to the development of medications that alleviate pain and reduce inflammation. Additionally, it is utilized in the manufacture of fragrances and flavors, where it imparts unique aromatic properties to perfumes and food products. In the field of polymer chemistry, it acts as a building block for creating specialized resins and coatings, enhancing their durability and performance. Its versatility also extends to research laboratories, where it is employed in the study of chemical reactions and the development of new synthetic pathways.
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