Methyl hydrazidodicarboxylate

99%

Reagent Code: #209899
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CAS Number 17643-54-8

science Other reagents with same CAS 17643-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.12 g/mol
Formula C₄H₈N₂O₄
badge Registry Numbers
MDL Number MFCD00216943
thermostat Physical Properties
Melting Point 129-131 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of pyrazoles and triazoles, which are important structures in pharmaceuticals and agrochemicals. It participates in cyclization reactions to form nitrogen-containing rings, making it valuable in drug discovery and development. Its reactivity allows for the introduction of functionalized hydrazine moieties, enabling the design of bioactive molecules with potential antiviral, antibacterial, or anticancer properties. Also employed in research settings for the development of novel organic transformations and as a building block in combinatorial chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿37,620.00
Methyl hydrazidodicarboxylate
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Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of pyrazoles and triazoles, which are important structures in pharmaceuticals and agrochemicals. It participates in cyclization reactions to form nitrogen-containing rings, making it valuable in drug discovery and development. Its reactivity allows for the introduction of functionalized hydrazine moieties, enabling the design of bioactive molecules with potential antiviral, antibacterial, or anticancer

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of pyrazoles and triazoles, which are important structures in pharmaceuticals and agrochemicals. It participates in cyclization reactions to form nitrogen-containing rings, making it valuable in drug discovery and development. Its reactivity allows for the introduction of functionalized hydrazine moieties, enabling the design of bioactive molecules with potential antiviral, antibacterial, or anticancer properties. Also employed in research settings for the development of novel organic transformations and as a building block in combinatorial chemistry.

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