Isopropyl 1H-imidazole-1-carboxylate

98%

Reagent Code: #200911
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CAS Number 82998-18-3

science Other reagents with same CAS 82998-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₇H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD21336269
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a reagent in organic synthesis, particularly in the activation of carboxylic acids for amide bond formation. It facilitates peptide coupling reactions by generating active esters in situ, offering an alternative to traditional coupling agents. Its imidazole leaving group enhances reactivity under mild conditions, making it suitable for sensitive substrates. Also employed in the preparation of pharmaceutical intermediates where efficient acylation is required without racemization. Shows utility in medicinal chemistry for constructing heterocyclic compounds and functionalizing biomolecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿680.00
inventory 5g
10-20 days ฿3,090.00
inventory 25g
10-20 days ฿15,410.00
inventory 100g
10-20 days ฿53,570.00
Isopropyl 1H-imidazole-1-carboxylate
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Used as a reagent in organic synthesis, particularly in the activation of carboxylic acids for amide bond formation. It facilitates peptide coupling reactions by generating active esters in situ, offering an alternative to traditional coupling agents. Its imidazole leaving group enhances reactivity under mild conditions, making it suitable for sensitive substrates. Also employed in the preparation of pharmaceutical intermediates where efficient acylation is required without racemization. Shows utility in

Used as a reagent in organic synthesis, particularly in the activation of carboxylic acids for amide bond formation. It facilitates peptide coupling reactions by generating active esters in situ, offering an alternative to traditional coupling agents. Its imidazole leaving group enhances reactivity under mild conditions, making it suitable for sensitive substrates. Also employed in the preparation of pharmaceutical intermediates where efficient acylation is required without racemization. Shows utility in medicinal chemistry for constructing heterocyclic compounds and functionalizing biomolecules.

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