(R)-1,1,1-Trifluoro-2-propanol
97%
- Product Code: 78975
CAS:
17628-73-8
Molecular Weight: | 114.07 g./mol | Molecular Formula: | C₃H₅F₃O |
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EC Number: | MDL Number: | MFCD06797330 | |
Melting Point: | Boiling Point: | 67.0±35.0℃(Predicted) | |
Density: | 1.235±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
(R)-1,1,1-Trifluoro-2-propanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the compounds it is incorporated into. This chemical is particularly valuable in the production of enantiomerically pure drugs, where it serves as a key intermediate. Additionally, it is employed in the development of specialty chemicals and materials, including liquid crystals and polymers, due to its unique structural properties. Its application extends to research and development in organic chemistry, where it is utilized for studying stereoselective reactions and chiral catalysis.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | Colorless to Yellow Liquid |
PURITY | 96.5-100 |
Optical Rotation0.5 CHCl3 | 5 10 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿12,680.00 |
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(R)-1,1,1-Trifluoro-2-propanol
(R)-1,1,1-Trifluoro-2-propanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the compounds it is incorporated into. This chemical is particularly valuable in the production of enantiomerically pure drugs, where it serves as a key intermediate. Additionally, it is employed in the development of specialty chemicals and materials, including liquid crystals and polymers, due to its unique structural properties. Its application extends to research and development in organic chemistry, where it is utilized for studying stereoselective reactions and chiral catalysis.
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