5-Chloro-1H-indazole-3-carbaldehyde

≥95%

Reagent Code: #161868
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CAS Number 102735-84-2

science Other reagents with same CAS 102735-84-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.59 g/mol
Formula C₈H₅ClN₂O
badge Registry Numbers
MDL Number MFCD07781535
thermostat Physical Properties
Boiling Point 391.7±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and heterocyclic structure, enabling the formation of Schiff bases or other derivatives that exhibit biological activity. Commonly employed in research settings for designing new drug candidates targeting inflammatory diseases and neurodegenerative disorders. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,070.00
inventory 250mg
10-20 days ฿6,780.00
inventory 1g
10-20 days ฿13,570.00
inventory 5g
10-20 days ฿40,740.00

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5-Chloro-1H-indazole-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and heterocyclic structure, enabling the formation of Schiff bases or other derivatives that exhibit biological activity. Commonly employed in research settings for designing new drug candidates targeting inflammatory diseases and neurodegenerative disorders. Also utilized

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive aldehyde group and heterocyclic structure, enabling the formation of Schiff bases or other derivatives that exhibit biological activity. Commonly employed in research settings for designing new drug candidates targeting inflammatory diseases and neurodegenerative disorders. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and selectivity.

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