2-Bromo-5-(difluoromethoxy)benzaldehyde

97%

Reagent Code: #152843
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CAS Number 1504952-98-0

science Other reagents with same CAS 1504952-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.0249 g/mol
Formula C₈H₅BrF₂O₂
badge Registry Numbers
MDL Number MFCD24131095
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for agrochemicals and medicinal compounds. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Commonly employed in cross-coupling reactions, it helps build carbon-carbon bonds in the production of fluorinated compounds with enhanced metabolic stability and bioavailability. Also utilized in the manufacture of herbicides and fungicides due to the favorable reactivity of the bromine and aldehyde groups.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,300.00
250mg
10-20 days ฿2,850.00
1g
10-20 days ฿8,920.00
5g
10-20 days ฿41,610.00
2-Bromo-5-(difluoromethoxy)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for agrochemicals and medicinal compounds. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Commonly employed in cross-coupling reactions, it helps build carbon-carbon bonds in the production of fluorinated compounds with enhanced metabolic stability and bioavailability. Also utilized in the manufacture of herbicides and fungi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for agrochemicals and medicinal compounds. Its structure allows for selective functionalization, making it valuable in creating complex organic molecules. Commonly employed in cross-coupling reactions, it helps build carbon-carbon bonds in the production of fluorinated compounds with enhanced metabolic stability and bioavailability. Also utilized in the manufacture of herbicides and fungicides due to the favorable reactivity of the bromine and aldehyde groups.

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