1,1,1-Trifluoro-3-methyl-2-butanol
≥97%
- Product Code: 78989
CAS:
382-02-5
Molecular Weight: | 142.12 g./mol | Molecular Formula: | C₅H₉F₃O |
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EC Number: | MDL Number: | MFCD00462511 | |
Melting Point: | Boiling Point: | 98-104 ℃ | |
Density: | 1.149 g/ml at 25 ℃ | Storage Condition: | 2-8°C, sealed and dry |
Product Description:
This chemical is primarily utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique trifluoromethyl group makes it valuable in the development of compounds with enhanced biological activity and stability. It is often employed in the production of active ingredients for drugs targeting specific diseases, including anti-inflammatory and anti-infective agents. Additionally, it serves as a building block in the creation of advanced materials, such as specialty polymers and coatings, where its fluorine content contributes to improved durability and resistance to harsh environmental conditions. In the field of organic chemistry, it is used as a reagent or precursor in complex synthetic pathways, particularly in the introduction of fluorine atoms into target molecules.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿5,724.00 |
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5.000 | 10-20 days | ฿22,707.00 |
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1,1,1-Trifluoro-3-methyl-2-butanol
This chemical is primarily utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique trifluoromethyl group makes it valuable in the development of compounds with enhanced biological activity and stability. It is often employed in the production of active ingredients for drugs targeting specific diseases, including anti-inflammatory and anti-infective agents. Additionally, it serves as a building block in the creation of advanced materials, such as specialty polymers and coatings, where its fluorine content contributes to improved durability and resistance to harsh environmental conditions. In the field of organic chemistry, it is used as a reagent or precursor in complex synthetic pathways, particularly in the introduction of fluorine atoms into target molecules.
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