(2R)-1-[3-(Trifluoromethyl)phenoxy]-3-butyn-2-ol

≥95%

Reagent Code: #229085
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CAS Number 301834-96-8

science Other reagents with same CAS 301834-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.1832 g/mol
Formula C₁₁H₉F₃O₂
thermostat Physical Properties
Boiling Point 299.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.292±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex organic compounds with high selectivity, making it valuable in medicinal chemistry for drug discovery. The presence of both alkyne and alcohol functional groups allows for further chemical modifications, including coupling reactions and derivatization, commonly employed in creating targeted therapies for cancer and inflammatory diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿16,000.00
inventory 10g
10-20 days ฿80,000.00
inventory 5g
10-20 days ฿48,000.00
(2R)-1-[3-(Trifluoromethyl)phenoxy]-3-butyn-2-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex organic compounds with high selectivity, making it valuable in medicinal chemistry for drug discovery. The presence of both alkyne and alcohol functional groups allows for further chemical modifications, including coupling reactions and derivatization, commonly employed in creating targeted therapies for cancer

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex organic compounds with high selectivity, making it valuable in medicinal chemistry for drug discovery. The presence of both alkyne and alcohol functional groups allows for further chemical modifications, including coupling reactions and derivatization, commonly employed in creating targeted therapies for cancer and inflammatory diseases.

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