4-(Thiophen-3-yl)-3-(trifluoromethyl)benzoic acid

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Reagent Code: #46517
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CAS Number 2340293-28-7

science Other reagents with same CAS 2340293-28-7

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Weight 272.2430 g/mol
Formula C₁₂H₇F₃O₂S
badge Registry Numbers
MDL Number MFCD31916168
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Storage room temperature

description Product Description

Used in the synthesis of pharmaceutical compounds, particularly in the development of small molecule drugs targeting specific biological pathways. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) with potential therapeutic applications, such as anti-inflammatory or anticancer agents. The trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in drug design. The thiophen-3-yl moiety contributes to the molecule's unique structural properties for biological interactions. Additionally, it is employed in organic chemistry research for studying structure-activity relationships (SAR) in medicinal chemistry projects.

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inventory 50mg
10-20 days ฿3,006.00

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4-(Thiophen-3-yl)-3-(trifluoromethyl)benzoic acid
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Used in the synthesis of pharmaceutical compounds, particularly in the development of small molecule drugs targeting specific biological pathways. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) with potential therapeutic applications, such as anti-inflammatory or anticancer agents. The trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in drug design. The thiophen-3-yl moiety contributes to the molecule's unique struct

Used in the synthesis of pharmaceutical compounds, particularly in the development of small molecule drugs targeting specific biological pathways. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) with potential therapeutic applications, such as anti-inflammatory or anticancer agents. The trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in drug design. The thiophen-3-yl moiety contributes to the molecule's unique structural properties for biological interactions. Additionally, it is employed in organic chemistry research for studying structure-activity relationships (SAR) in medicinal chemistry projects.

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