2-(3-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol
≥95%
- Product Code: 85094
CAS:
2402-67-7
Molecular Weight: | 259.15 g./mol | Molecular Formula: | C₉H₇F₆NO |
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EC Number: | MDL Number: | MFCD17015636 | |
Melting Point: | Boiling Point: | 291.1°C at 760 mmHg | |
Density: | 1.505g/cm3 | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in the synthesis of advanced materials and specialty chemicals. Its unique structure, featuring both an amino group and hexafluoropropanol moiety, makes it a valuable intermediate in the production of high-performance polymers and coatings. These materials are often employed in industries requiring exceptional chemical resistance, thermal stability, and low surface energy, such as aerospace, electronics, and automotive sectors. Additionally, it serves as a building block in the development of pharmaceuticals and agrochemicals, where its fluorine-containing group can enhance the biological activity and stability of the final compounds. Its application in organic synthesis also extends to the creation of ligands and catalysts used in asymmetric catalysis, contributing to the production of chiral molecules in fine chemical manufacturing.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿11,664.00 |
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0.250 | 10-20 days | ฿18,756.00 |
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1.000 | 10-20 days | ฿46,908.00 |
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2-(3-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol
This chemical is primarily utilized in the synthesis of advanced materials and specialty chemicals. Its unique structure, featuring both an amino group and hexafluoropropanol moiety, makes it a valuable intermediate in the production of high-performance polymers and coatings. These materials are often employed in industries requiring exceptional chemical resistance, thermal stability, and low surface energy, such as aerospace, electronics, and automotive sectors. Additionally, it serves as a building block in the development of pharmaceuticals and agrochemicals, where its fluorine-containing group can enhance the biological activity and stability of the final compounds. Its application in organic synthesis also extends to the creation of ligands and catalysts used in asymmetric catalysis, contributing to the production of chiral molecules in fine chemical manufacturing.
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