Ethyl 3-bromo-2,2-difluoropropionate

≥95.0%

Reagent Code: #184106
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CAS Number 111773-24-1

science Other reagents with same CAS 111773-24-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.01 g/mol
Formula C₅H₇BrF₂O₂
badge Registry Numbers
MDL Number MFCD15144891
thermostat Physical Properties
Boiling Point 157.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.564±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive bromo and ester functional groups. The presence of fluorine atoms enhances metabolic stability and lipophilicity in final active compounds. Commonly employed in the preparation of fluorinated building blocks for drug discovery, particularly in the development of protease inhibitors and kinase inhibitors. Also utilized in the synthesis of chiral fluorinated molecules through asymmetric transformations. Its versatility makes it valuable in medicinal chemistry for structure-activity relationship (SAR) studies involving fluorinated analogs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,970.00
inventory 5g
10-20 days ฿8,180.00

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Ethyl 3-bromo-2,2-difluoropropionate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive bromo and ester functional groups. The presence of fluorine atoms enhances metabolic stability and lipophilicity in final active compounds. Commonly employed in the preparation of fluorinated building blocks for drug discovery, particularly in the development of protease inhibitors and kinase inhibitors. Also utilized in the synthesis of chiral fluorinated molecules through asymmetric transfor

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its reactive bromo and ester functional groups. The presence of fluorine atoms enhances metabolic stability and lipophilicity in final active compounds. Commonly employed in the preparation of fluorinated building blocks for drug discovery, particularly in the development of protease inhibitors and kinase inhibitors. Also utilized in the synthesis of chiral fluorinated molecules through asymmetric transformations. Its versatility makes it valuable in medicinal chemistry for structure-activity relationship (SAR) studies involving fluorinated analogs.

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