tert-Butyl (6-bromonaphthalen-2-yl)(methyl)carbamate

95%

Reagent Code: #87910
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CAS Number 1388628-76-9

science Other reagents with same CAS 1388628-76-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.22 g/mol
Formula C₁₆H₁₈BrNO₂
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in the preparation of pharmaceutical compounds, where the bromine atom serves as a reactive site for further functionalization through coupling reactions, such as Suzuki or Buchwald-Hartwig reactions. The tert-butyl carbamate group provides protection for the amine functionality, which can be deprotected later in the synthesis process. This compound is also employed in the research and development of bioactive molecules, including potential drug candidates targeting various diseases. Its structural features make it a versatile building block in medicinal chemistry and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,020.00

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tert-Butyl (6-bromonaphthalen-2-yl)(methyl)carbamate
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This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in the preparation of pharmaceutical compounds, where the bromine atom serves as a reactive site for further functionalization through coupling reactions, such as Suzuki or Buchwald-Hartwig reactions. The tert-butyl carbamate group provides protection for the amine functionality, which can be deprotected later in the synthesis process. This compound is als

This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in the preparation of pharmaceutical compounds, where the bromine atom serves as a reactive site for further functionalization through coupling reactions, such as Suzuki or Buchwald-Hartwig reactions. The tert-butyl carbamate group provides protection for the amine functionality, which can be deprotected later in the synthesis process. This compound is also employed in the research and development of bioactive molecules, including potential drug candidates targeting various diseases. Its structural features make it a versatile building block in medicinal chemistry and materials science.

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