Methyl4-formyl-2-(trifluoromethyl)benzoate

98%

Reagent Code: #213761
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CAS Number 959632-16-7

science Other reagents with same CAS 959632-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.16 g/mol
Formula C₁₀H₇F₃O₃
badge Registry Numbers
MDL Number MFCD27935000
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in building complex organic molecules. Commonly employed in reactions such as condensations, reductions, and cross-coupling processes to introduce aromatic and fluorinated moieties into target structures. Also utilized in the preparation of fluorinated analogs in medicinal chemistry due to the presence of the trifluoromethyl group, which can enhance metabolic stability and lipophilicity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿10,330.00
250mg
10-20 days ฿17,510.00
1g
10-20 days ฿45,220.00
5g
10-20 days ฿67,710.00
Methyl4-formyl-2-(trifluoromethyl)benzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in building complex organic molecules. Commonly employed in reactions such as condensations, reductions, and cross-coupling processes to introduce aromatic and fluorinated moieties into target structures. Also utilized in the preparation of fluorinated analogs
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in building complex organic molecules. Commonly employed in reactions such as condensations, reductions, and cross-coupling processes to introduce aromatic and fluorinated moieties into target structures. Also utilized in the preparation of fluorinated analogs in medicinal chemistry due to the presence of the trifluoromethyl group, which can enhance metabolic stability and lipophilicity.
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