4-(Trifluoromethylthio)benzyl bromide

97.0%

Reagent Code: #240018
label
Alias 4-(trifluoromethylthio)benzyl bromide; 4-(trifluoromethylthio)benzyl bromide; α-bromo-4-(trifluoromethylthio)toluene
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CAS Number 21101-63-3

science Other reagents with same CAS 21101-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.1 g/mol
Formula C₈H₆BrF₃S
badge Registry Numbers
MDL Number MFCD00129189
thermostat Physical Properties
Melting Point 53-57 °C(lit.)
Boiling Point 115-118°C 13mm
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity. Its trifluoromethylthio group contributes to improved bioavailability and binding affinity in biologically active molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors and antifungal agents. Also utilized in the fabrication of functionalized polymers and as a building block in medicinal chemistry for structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿690.00
inventory 250mg
10-20 days ฿1,060.00
4-(Trifluoromethylthio)benzyl bromide
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity. Its trifluoromethylthio group contributes to improved bioavailability and binding affinity in biologically active molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors and antifungal agents. Also utilized in the fabrication of functionalized polymers and as a building block in medicinal chem

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity. Its trifluoromethylthio group contributes to improved bioavailability and binding affinity in biologically active molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors and antifungal agents. Also utilized in the fabrication of functionalized polymers and as a building block in medicinal chemistry for structure-activity relationship studies.

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