Ethyl tribromoacetate

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Reagent Code: #180838
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CAS Number 599-99-5

science Other reagents with same CAS 599-99-5

blur_circular Chemical Specifications

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Weight 324.79 g/mol
Formula C₄H₅Br₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Ethyl tribromoacetate is used as a reagent in organic synthesis, particularly for introducing the tribromoacetyl group in the preparation of intermediates such as α,α,α-tribromoacetate derivatives for various pharmaceuticals and agrochemicals. It is also employed in the synthesis of heterocyclic compounds and in bromination reactions due to its ability to generate dibromocarbene or introduce bromine atoms into organic molecules. Its high reactivity makes it valuable in the development of active ingredients in crop protection products and in the construction of complex organic frameworks through carbon-chain elongation or functional group transformation.

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inventory 5g
10-20 days ฿14,400.00

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Ethyl tribromoacetate
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Ethyl tribromoacetate is used as a reagent in organic synthesis, particularly for introducing the tribromoacetyl group in the preparation of intermediates such as α,α,α-tribromoacetate derivatives for various pharmaceuticals and agrochemicals. It is also employed in the synthesis of heterocyclic compounds and in bromination reactions due to its ability to generate dibromocarbene or introduce bromine atoms into organic molecules. Its high reactivity makes it valuable in the development of active ingredien

Ethyl tribromoacetate is used as a reagent in organic synthesis, particularly for introducing the tribromoacetyl group in the preparation of intermediates such as α,α,α-tribromoacetate derivatives for various pharmaceuticals and agrochemicals. It is also employed in the synthesis of heterocyclic compounds and in bromination reactions due to its ability to generate dibromocarbene or introduce bromine atoms into organic molecules. Its high reactivity makes it valuable in the development of active ingredients in crop protection products and in the construction of complex organic frameworks through carbon-chain elongation or functional group transformation.

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