tert-Butyl (4-bromophenyl)(methyl)carbamate

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Reagent Code: #36926
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CAS Number 639520-70-0

science Other reagents with same CAS 639520-70-0

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Weight 286.1649 g/mol
Formula C₁₂H₁₆BrNO₂
badge Registry Numbers
MDL Number MFCD12913712
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description Product Description

Primarily used in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into complex molecules. In medicinal chemistry, it is employed to create compounds with potential therapeutic properties, such as enzyme inhibitors or receptor modulators. Additionally, its bromophenyl group makes it a useful building block in cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of more complex organic structures. Its tert-butyl group provides steric protection, enhancing selectivity in certain chemical transformations.

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inventory 250mg
10-20 days ฿1,026.00

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tert-Butyl (4-bromophenyl)(methyl)carbamate
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Primarily used in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into complex molecules. In medicinal chemistry, it is employed to create compounds with potential therapeutic properties, such as enzyme inhibitors or receptor modulators. Additionally, its bromophenyl group makes i

Primarily used in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into complex molecules. In medicinal chemistry, it is employed to create compounds with potential therapeutic properties, such as enzyme inhibitors or receptor modulators. Additionally, its bromophenyl group makes it a useful building block in cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of more complex organic structures. Its tert-butyl group provides steric protection, enhancing selectivity in certain chemical transformations.

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