1-[(Phenoxycarbonyl)oxy]-1H-pyrrole-2,5-dione

Reagent Code: #223771
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CAS Number 60361-89-9

science Other reagents with same CAS 60361-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.18 g/mol
Formula C₁₁H₇NO₅
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MDL Number MFCD00096931
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a highly reactive intermediate in organic synthesis, particularly in the preparation of carbamates and urethanes through reaction with amines. It acts as an activating agent for carboxylic acids, facilitating peptide coupling and esterification under mild conditions. Commonly employed in pharmaceutical manufacturing to introduce the phenoxycarbonyl protecting group. Also utilized in polymer chemistry for modifying resins and crosslinking agents due to its ability to form stable linkages with nucleophiles. Its high reactivity makes it suitable for use in controlled environments where fast acylation is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿25,650.00
1-[(Phenoxycarbonyl)oxy]-1H-pyrrole-2,5-dione
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Used as a highly reactive intermediate in organic synthesis, particularly in the preparation of carbamates and urethanes through reaction with amines. It acts as an activating agent for carboxylic acids, facilitating peptide coupling and esterification under mild conditions. Commonly employed in pharmaceutical manufacturing to introduce the phenoxycarbonyl protecting group. Also utilized in polymer chemistry for modifying resins and crosslinking agents due to its ability to form stable linkages with nucl

Used as a highly reactive intermediate in organic synthesis, particularly in the preparation of carbamates and urethanes through reaction with amines. It acts as an activating agent for carboxylic acids, facilitating peptide coupling and esterification under mild conditions. Commonly employed in pharmaceutical manufacturing to introduce the phenoxycarbonyl protecting group. Also utilized in polymer chemistry for modifying resins and crosslinking agents due to its ability to form stable linkages with nucleophiles. Its high reactivity makes it suitable for use in controlled environments where fast acylation is required.

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