Tetrahydrofurfuryl bromide

95%

Reagent Code: #240390
label
Alias 2-Bromomethyltetrahydrofuran
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CAS Number 1192-30-9

science Other reagents with same CAS 1192-30-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.03 g/mol
Formula C₅H₉BrO
badge Registry Numbers
MDL Number MFCD00016894
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Tetrahydrofurfuryl bromide is primarily used as an intermediate in organic synthesis. It serves as an alkylating agent in the preparation of pharmaceuticals, agrochemicals, and specialty polymers. Its reactivity allows for the introduction of the tetrahydrofurfuryl group into various molecules, enhancing solubility or altering biological activity in drug development. It is also employed in the synthesis of surfactants and functionalized materials where ether or amine derivatives are needed. Due to the presence of the bromide leaving group, it readily participates in substitution reactions, making it valuable in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 25g
10-20 days ฿3,200.00
inventory 100g
10-20 days ฿8,990.00
inventory 500g
10-20 days ฿28,990.00
inventory 5g
10-20 days ฿1,060.00
Tetrahydrofurfuryl bromide
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Tetrahydrofurfuryl bromide is primarily used as an intermediate in organic synthesis. It serves as an alkylating agent in the preparation of pharmaceuticals, agrochemicals, and specialty polymers. Its reactivity allows for the introduction of the tetrahydrofurfuryl group into various molecules, enhancing solubility or altering biological activity in drug development. It is also employed in the synthesis of surfactants and functionalized materials where ether or amine derivatives are needed. Due to the pr

Tetrahydrofurfuryl bromide is primarily used as an intermediate in organic synthesis. It serves as an alkylating agent in the preparation of pharmaceuticals, agrochemicals, and specialty polymers. Its reactivity allows for the introduction of the tetrahydrofurfuryl group into various molecules, enhancing solubility or altering biological activity in drug development. It is also employed in the synthesis of surfactants and functionalized materials where ether or amine derivatives are needed. Due to the presence of the bromide leaving group, it readily participates in substitution reactions, making it valuable in multi-step synthetic routes.

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