2-Methoxy-4-(trifluoromethyl)benzyl bromide

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Reagent Code: #116926
label
Alias 2-Methoxy-4-(trifluoromethyl)benzyl bromide, JRD; 2-methoxy-4-(trifluoromethyl)benzyl bromide; 4-trifluoromethoxy-2-methoxy Benzyl bromide
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CAS Number 886500-59-0

science Other reagents with same CAS 886500-59-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.06 g/mol
Formula C₉H₈BrF₃O
thermostat Physical Properties
Melting Point 42-45℃
Boiling Point 239.7±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.524±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its benzyl bromide group makes it a versatile alkylating agent, enabling the introduction of the 2-methoxy-4-(trifluoromethyl)benzyl moiety into various target molecules. This is particularly valuable in the development of active ingredients for drugs, where the trifluoromethyl group can enhance metabolic stability and bioavailability. Additionally, it finds application in the synthesis of specialty chemicals and advanced materials, where its unique structure contributes to specific desired properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿32,652.00
inventory 1g
10-20 days ฿7,407.00

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2-Methoxy-4-(trifluoromethyl)benzyl bromide
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its benzyl bromide group makes it a versatile alkylating agent, enabling the introduction of the 2-methoxy-4-(trifluoromethyl)benzyl moiety into various target molecules. This is particularly valuable in the development of active ingredients for drugs, where the trifluoromethyl group can enhance metabolic stability and bioavailability. Additionally, it finds application

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its benzyl bromide group makes it a versatile alkylating agent, enabling the introduction of the 2-methoxy-4-(trifluoromethyl)benzyl moiety into various target molecules. This is particularly valuable in the development of active ingredients for drugs, where the trifluoromethyl group can enhance metabolic stability and bioavailability. Additionally, it finds application in the synthesis of specialty chemicals and advanced materials, where its unique structure contributes to specific desired properties.

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