tert-butyl (3-methoxyphenyl)carbamate

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Reagent Code: #242342
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CAS Number 60144-52-7

science Other reagents with same CAS 60144-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.27 g/mol
Formula C₁₂H₁₇NO₃
badge Registry Numbers
MDL Number MFCD07127720
thermostat Physical Properties
Melting Point 55 - 60 ℃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a protected aniline derivative, where the tert-butoxycarbonyl (Boc) group stabilizes the nitrogen during reactions, allowing selective functionalization on the aromatic ring. The methoxy group enhances electron density, making it useful in cross-coupling reactions, such as Suzuki or Heck reactions. Commonly employed in the development of bioactive compounds, including drug candidates targeting central nervous system disorders and inflammatory conditions. Its stability under various reaction conditions makes it valuable in multi-step synthesis.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,970.00
inventory 100g
10-20 days ฿7,350.00

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tert-butyl (3-methoxyphenyl)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 aniline derivative, where the tert-butoxycarbonyl (Boc) group stabilizes the nitrogen during reactions, allowing selective functionalization on the aromatic ring. The methoxy group enhances electron density, making it useful in cross-coupling reactions, such as Suzuki or Heck reactions. Commonly employed in the development of bioactive compounds, including

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a protected aniline derivative, where the tert-butoxycarbonyl (Boc) group stabilizes the nitrogen during reactions, allowing selective functionalization on the aromatic ring. The methoxy group enhances electron density, making it useful in cross-coupling reactions, such as Suzuki or Heck reactions. Commonly employed in the development of bioactive compounds, including drug candidates targeting central nervous system disorders and inflammatory conditions. Its stability under various reaction conditions makes it valuable in multi-step synthesis.

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