tert-Butyl (4-bromocyclohexyl)carbamate

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Reagent Code: #145467
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CAS Number 1353963-71-9

science Other reagents with same CAS 1353963-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.19 g/mol
Formula C₁₁H₂₀BrNO₂
thermostat Physical Properties
Boiling Point 340.5±31.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a protected amine derivative, enabling selective reactions at other functional sites without interference from the amine group. Commonly employed in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and anti-inflammatory agents. Its stability under various reaction conditions makes it valuable in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,510.00
inventory 25mg
10-20 days ฿3,130.00

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tert-Butyl (4-bromocyclohexyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a protected amine derivative, enabling selective reactions at other functional sites without interference from the amine group. Commonly employed in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and anti-inflammatory agents. Its stability under various reaction conditions makes it valuable in mul

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a protected amine derivative, enabling selective reactions at other functional sites without interference from the amine group. Commonly employed in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and anti-inflammatory agents. Its stability under various reaction conditions makes it valuable in multi-step synthetic routes.

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