S-(trifluoromethyl) 2-bromobenzothioate

97%

Reagent Code: #236464
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CAS Number 2376271-51-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.084 g/mol
Formula C₈H₄BrF₃OS
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfur-containing bioactive molecules. Its trifluoromethyl and bromo functional groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex organic frameworks. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the enhanced metabolic stability imparted by the trifluoromethyl group. Also utilized in the design of novel pesticides, where the benzothioate scaffold contributes to target specificity and potency.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,950.00
S-(trifluoromethyl) 2-bromobenzothioate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfur-containing bioactive molecules. Its trifluoromethyl and bromo functional groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex organic frameworks. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the enhanced metabolic stability imparted by the trifluoromethyl group. Also utilized

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfur-containing bioactive molecules. Its trifluoromethyl and bromo functional groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex organic frameworks. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the enhanced metabolic stability imparted by the trifluoromethyl group. Also utilized in the design of novel pesticides, where the benzothioate scaffold contributes to target specificity and potency.

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