2-(Bromomethyl)-1,1-difluorocyclopropane

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Reagent Code: #153529
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CAS Number 77613-65-1

science Other reagents with same CAS 77613-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.98 g/mol
Formula C₄H₅BrF₂
badge Registry Numbers
MDL Number MFCD06797749
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its unique strained cyclopropane ring combined with bromine and difluoromethylene groups allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in alkylation reactions where the bromomethyl group acts as an electrophilic site for nucleophilic substitution. Also utilized in the preparation of fluorinated analogs of natural products to enhance metabolic stability and lipophilicity. Its reactivity profile supports use in cross-coupling reactions and ring-opening transformations for developing complex fluorinated structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,560.00
inventory 250mg
10-20 days ฿9,450.00
inventory 1g
10-20 days ฿25,510.00
inventory 5g
10-20 days ฿98,120.00

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2-(Bromomethyl)-1,1-difluorocyclopropane
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Used primarily as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its unique strained cyclopropane ring combined with bromine and difluoromethylene groups allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in alkylation reactions where the bromomethyl group acts as an electrophilic site for nucleophilic substitution. Also utilized in the preparation of fluorinated analogs of natural pr

Used primarily as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its unique strained cyclopropane ring combined with bromine and difluoromethylene groups allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in alkylation reactions where the bromomethyl group acts as an electrophilic site for nucleophilic substitution. Also utilized in the preparation of fluorinated analogs of natural products to enhance metabolic stability and lipophilicity. Its reactivity profile supports use in cross-coupling reactions and ring-opening transformations for developing complex fluorinated structures.

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