tert-Butyl (1-(3-bromophenyl)ethyl)carbamate
95%
- Product Code: 36118
CAS:
375853-98-8
Molecular Weight: | 300.1915 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₂ |
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EC Number: | MDL Number: | MFCD12913697 | |
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Density: | Storage Condition: | room temperature |
Product Description:
tert-Butyl (1-(3-bromophenyl)ethyl)carbamate is primarily used in organic synthesis as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it a valuable building block for constructing more complex molecules. The compound is often employed in the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds targeting neurological disorders, cancer, or infectious diseases. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and optimization. In agrochemical research, it may serve as a precursor for the development of herbicides, fungicides, or insecticides, leveraging its aromatic and carbamate functionalities.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,265.00 |
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tert-Butyl (1-(3-bromophenyl)ethyl)carbamate
tert-Butyl (1-(3-bromophenyl)ethyl)carbamate is primarily used in organic synthesis as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it a valuable building block for constructing more complex molecules. The compound is often employed in the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds targeting neurological disorders, cancer, or infectious diseases. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and optimization. In agrochemical research, it may serve as a precursor for the development of herbicides, fungicides, or insecticides, leveraging its aromatic and carbamate functionalities.
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