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

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Reagent Code: #148406
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CAS Number 99207-32-6

science Other reagents with same CAS 99207-32-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.28 g/mol
Formula C₁₀H₂₁NO₃
badge Registry Numbers
MDL Number MFCD09953073
thermostat Physical Properties
Boiling Point 284.2±19.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a protected intermediate in organic synthesis, particularly in the pharmaceutical industry. The tert-butyl carbamate group acts as a protecting group for amines, allowing selective reaction at other functional sites. The hydroxyl group can be further modified through esterification or ether formation, enabling incorporation into complex molecules. Commonly employed in the synthesis of bioactive compounds, including drug candidates targeting central nervous system disorders and metabolic diseases. Its stability under a variety of reaction conditions makes it valuable in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,320.00
inventory 250mg
10-20 days ฿1,600.00
inventory 1g
10-20 days ฿4,070.00
inventory 5g
10-20 days ฿17,540.00
inventory 25g
10-20 days ฿46,320.00

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tert-Butyl (4-hydroxybutyl)(methyl)carbamate
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Used as a protected intermediate in organic synthesis, particularly in the pharmaceutical industry. The tert-butyl carbamate group acts as a protecting group for amines, allowing selective reaction at other functional sites. The hydroxyl group can be further modified through esterification or ether formation, enabling incorporation into complex molecules. Commonly employed in the synthesis of bioactive compounds, including drug candidates targeting central nervous system disorders and metabolic diseases.

Used as a protected intermediate in organic synthesis, particularly in the pharmaceutical industry. The tert-butyl carbamate group acts as a protecting group for amines, allowing selective reaction at other functional sites. The hydroxyl group can be further modified through esterification or ether formation, enabling incorporation into complex molecules. Commonly employed in the synthesis of bioactive compounds, including drug candidates targeting central nervous system disorders and metabolic diseases. Its stability under a variety of reaction conditions makes it valuable in multi-step synthetic routes.

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