2-(4-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

98%

  • Product Code: 72273
  CAS:    722-92-9
Molecular Weight: 259.15 g./mol Molecular Formula: C₉H₇F₆NO
EC Number: MDL Number:
Melting Point: 147-152°C Boiling Point: 292.9°C
Density: Storage Condition: 2-8°C
Product Description: This compound 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 unique structure, featuring both an amino group and a hexafluoropropanol moiety, makes it particularly valuable in the development of compounds with enhanced biological activity and stability. Additionally, it is employed in the creation of advanced materials, such as specialty polymers and coatings, due to its ability to impart desirable properties like chemical resistance and thermal stability. In research settings, it is often used as a building block for the synthesis of complex molecules, aiding in the exploration of new chemical reactions and pathways.
Product Specification:
Test Specification
APPEARANCE White to cream or pale brown Powder
PURITY 97.5-100
MELTING POINT 147-152
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿300.00
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-
10.000 10-20 days ฿1,950.00
+
-
50.000 10-20 days ฿9,620.00
+
-
2-(4-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol
This compound 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 unique structure, featuring both an amino group and a hexafluoropropanol moiety, makes it particularly valuable in the development of compounds with enhanced biological activity and stability. Additionally, it is employed in the creation of advanced materials, such as specialty polymers and coatings, due to its ability to impart desirable properties like chemical resistance and thermal stability. In research settings, it is often used as a building block for the synthesis of complex molecules, aiding in the exploration of new chemical reactions and pathways.
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