1, 3-Dibromo-3-methylbutan-2-one

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Reagent Code: #178038
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CAS Number 1518-06-5

science Other reagents with same CAS 1518-06-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.92 g/mol
Formula C₅H₈Br₂O
badge Registry Numbers
MDL Number MFCD21602529
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and agrochemicals. Its reactive bromine atoms allow for substitution reactions, making it valuable in building complex molecular structures. It is also employed in the synthesis of heterocyclic compounds and bioactive molecules, where it serves as a building block for introducing functional groups. Due to its alkylating properties, it can modify organic frameworks in the development of active ingredients in crop protection products. Additionally, it finds use in research laboratories for studying reaction mechanisms involving alpha-halo ketones.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,330.00
inventory 250mg
10-20 days ฿5,380.00
inventory 1g
10-20 days ฿16,830.00
inventory 5g
10-20 days ฿78,560.00

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1, 3-Dibromo-3-methylbutan-2-one
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and agrochemicals. Its reactive bromine atoms allow for substitution reactions, making it valuable in building complex molecular structures. It is also employed in the synthesis of heterocyclic compounds and bioactive molecules, where it serves as a building block for introducing functional groups. Due to its alkylating properties, it can modify organic frameworks in the developmen

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and agrochemicals. Its reactive bromine atoms allow for substitution reactions, making it valuable in building complex molecular structures. It is also employed in the synthesis of heterocyclic compounds and bioactive molecules, where it serves as a building block for introducing functional groups. Due to its alkylating properties, it can modify organic frameworks in the development of active ingredients in crop protection products. Additionally, it finds use in research laboratories for studying reaction mechanisms involving alpha-halo ketones.

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