tert-Butyl cyclopent-3-en-1-ylcarbamate

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Reagent Code: #145138
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CAS Number 193751-54-1

science Other reagents with same CAS 193751-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.25 g/mol
Formula C₁₀H₁₇NO₂
thermostat Physical Properties
Boiling Point 268.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization of the cyclopentene ring, making it valuable in building complex molecules. Commonly employed in the development of bioactive compounds where a protected amine group is required, enabling controlled deprotection and coupling reactions. Also utilized in medicinal chemistry for designing enzyme inhibitors and receptor ligands due to its conformational rigidity and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,160.00
inventory 250mg
10-20 days ฿1,280.00
inventory 5g
10-20 days ฿12,800.00
inventory 10g
10-20 days ฿20,800.00
inventory 25g
10-20 days ฿43,200.00
inventory 1g
10-20 days ฿3,060.00
inventory 50g
10-20 days ฿72,000.00

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tert-Butyl cyclopent-3-en-1-ylcarbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization of the cyclopentene ring, making it valuable in building complex molecules. Commonly employed in the development of bioactive compounds where a protected amine group is required, enabling controlled deprotection and coupling reactions. Also utilized in medicinal chemistry for designing enzyme inhibitors and receptor ligands due to its con

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization of the cyclopentene ring, making it valuable in building complex molecules. Commonly employed in the development of bioactive compounds where a protected amine group is required, enabling controlled deprotection and coupling reactions. Also utilized in medicinal chemistry for designing enzyme inhibitors and receptor ligands due to its conformational rigidity and stability under various reaction conditions.

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