ethyl 2-diazopropanoate

95%

Reagent Code: #184957
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CAS Number 6111-99-5

science Other reagents with same CAS 6111-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.13 g/mol
Formula C₅H₈N₂O₂
inventory_2 Storage & Handling
Density 1.086 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used primarily as a diazo compound in organic synthesis, it serves as a key reagent for homologation reactions, enabling the extension of carbon chains. It is especially valuable in the preparation of cyclopropanes through cyclopropanation reactions with alkenes, often catalyzed by transition metals like rhodium or copper. Its ability to generate carbenes under mild conditions makes it useful in constructing complex ring systems found in pharmaceuticals and natural products. Additionally, it participates in X–H insertion reactions (where X = C, O, N) to form new carbon–heteroatom bonds, which are crucial in drug development and functional molecule design. Due to its reactivity, it is handled with care in controlled environments for safe and efficient transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,980.00
inventory 1g
10-20 days ฿43,980.00
inventory 5g
10-20 days ฿135,000.00

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ethyl 2-diazopropanoate
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Used primarily as a diazo compound in organic synthesis, it serves as a key reagent for homologation reactions, enabling the extension of carbon chains. It is especially valuable in the preparation of cyclopropanes through cyclopropanation reactions with alkenes, often catalyzed by transition metals like rhodium or copper. Its ability to generate carbenes under mild conditions makes it useful in constructing complex ring systems found in pharmaceuticals and natural products. Additionally, it participates

Used primarily as a diazo compound in organic synthesis, it serves as a key reagent for homologation reactions, enabling the extension of carbon chains. It is especially valuable in the preparation of cyclopropanes through cyclopropanation reactions with alkenes, often catalyzed by transition metals like rhodium or copper. Its ability to generate carbenes under mild conditions makes it useful in constructing complex ring systems found in pharmaceuticals and natural products. Additionally, it participates in X–H insertion reactions (where X = C, O, N) to form new carbon–heteroatom bonds, which are crucial in drug development and functional molecule design. Due to its reactivity, it is handled with care in controlled environments for safe and efficient transformations.

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