Diisopropyl hydrazine-1,2-dicarboxylate

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Reagent Code: #171080
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CAS Number 19740-72-8

science Other reagents with same CAS 19740-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.22 g/mol
Formula C₈H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD19443326
thermostat Physical Properties
Boiling Point 271.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and agrochemicals. It serves as a protecting group reagent for hydrazine moieties due to the stability provided by the ester groups. Commonly employed in the synthesis of heterocyclic compounds, including triazoles and pyrazoles, which are important scaffolds in drug discovery. Its reactivity allows for selective transformations in multi-step synthetic routes, making it valuable in research and development of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿730.00
inventory 1g
10-20 days ฿2,070.00
inventory 5g
10-20 days ฿8,490.00

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Diisopropyl hydrazine-1,2-dicarboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and agrochemicals. It serves as a protecting group reagent for hydrazine moieties due to the stability provided by the ester groups. Commonly employed in the synthesis of heterocyclic compounds, including triazoles and pyrazoles, which are important scaffolds in drug discovery. Its reactivity allows for selective transformations in multi-step synthetic routes, making it valuable in research

Used as a key intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and agrochemicals. It serves as a protecting group reagent for hydrazine moieties due to the stability provided by the ester groups. Commonly employed in the synthesis of heterocyclic compounds, including triazoles and pyrazoles, which are important scaffolds in drug discovery. Its reactivity allows for selective transformations in multi-step synthetic routes, making it valuable in research and development of bioactive molecules.

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