Diethyl 2-Diazomalonate

≥97%

Reagent Code: #176695
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CAS Number 5256-74-6

science Other reagents with same CAS 5256-74-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.17 g/mol
Formula C₇H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD00666477
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key reagent in organic synthesis, particularly in cyclopropanation reactions through metal-catalyzed decomposition. It transfers diazo groups to alkenes, forming cyclopropane derivatives important in pharmaceuticals and agrochemicals. Also employed in the preparation of β-lactams and other heterocyclic compounds via X-H insertion reactions (X = O, N, S). Its ability to generate carbenes under mild conditions makes it valuable in constructing complex molecular architectures. Handle with care due to explosive and toxic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,000.00

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Diethyl 2-Diazomalonate
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Used as a key reagent in organic synthesis, particularly in cyclopropanation reactions through metal-catalyzed decomposition. It transfers diazo groups to alkenes, forming cyclopropane derivatives important in pharmaceuticals and agrochemicals. Also employed in the preparation of β-lactams and other heterocyclic compounds via X-H insertion reactions (X = O, N, S). Its ability to generate carbenes under mild conditions makes it valuable in constructing complex molecular architectures. Handle with care due

Used as a key reagent in organic synthesis, particularly in cyclopropanation reactions through metal-catalyzed decomposition. It transfers diazo groups to alkenes, forming cyclopropane derivatives important in pharmaceuticals and agrochemicals. Also employed in the preparation of β-lactams and other heterocyclic compounds via X-H insertion reactions (X = O, N, S). Its ability to generate carbenes under mild conditions makes it valuable in constructing complex molecular architectures. Handle with care due to explosive and toxic properties.

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