4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide

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Reagent Code: #238268
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CAS Number 90434-92-7

science Other reagents with same CAS 90434-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.21 g/mol
Formula C₈H₁₂N₄O
badge Registry Numbers
MDL Number MFCD00611197
thermostat Physical Properties
Melting Point 176-179 °C
inventory_2 Storage & Handling
Density 1.331±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of bioactive molecules and pharmaceuticals. Its hydrazide functional group allows it to participate in condensation reactions, making it valuable for forming hydrazone derivatives, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. It is also employed in the development of heterocyclic compounds with potential central nervous system activity. Due to its structure, it serves as a building block in medicinal chemistry for designing new drug candidates, particularly in research focused on kinase inhibitors and neurological agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,950.00
inventory 1g
10-20 days ฿31,600.00

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4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of bioactive molecules and pharmaceuticals. Its hydrazide functional group allows it to participate in condensation reactions, making it valuable for forming hydrazone derivatives, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. It is also employed in the development of heterocyclic compounds with potential central nervous system activity. Due to its st

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of bioactive molecules and pharmaceuticals. Its hydrazide functional group allows it to participate in condensation reactions, making it valuable for forming hydrazone derivatives, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. It is also employed in the development of heterocyclic compounds with potential central nervous system activity. Due to its structure, it serves as a building block in medicinal chemistry for designing new drug candidates, particularly in research focused on kinase inhibitors and neurological agents.

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