Ethyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate

98%

Reagent Code: #185706
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CAS Number 146137-87-3

science Other reagents with same CAS 146137-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.23 g/mol
Formula C₁₁H₇F₃O₂S
badge Registry Numbers
MDL Number MFCD09027107
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of bioactive molecules due to the presence of both ester and trifluoromethyl groups, which enhance metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting neurological disorders and chronic pain. Also utilized in agrochemical research for developing new herbicides and pesticides owing to its electron-withdrawing properties and resistance to degradation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,250.00
inventory 5g
10-20 days ฿50,990.00
inventory 250mg
10-20 days ฿4,790.00
Ethyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of bioactive molecules due to the presence of both ester and trifluoromethyl groups, which enhance metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting neurological

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the design of bioactive molecules due to the presence of both ester and trifluoromethyl groups, which enhance metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates targeting neurological disorders and chronic pain. Also utilized in agrochemical research for developing new herbicides and pesticides owing to its electron-withdrawing properties and resistance to degradation.

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