6-Chloro-1H-indazole-3-carbaldehyde

≥95%

Reagent Code: #161869
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CAS Number 885521-37-9

science Other reagents with same CAS 885521-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.59 g/mol
Formula C₈H₅ClN₂O
badge Registry Numbers
MDL Number MFCD05663998
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 pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo functional group transformations, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing new active ingredients with potential pesticidal or fungicidal activity. Its structural features make it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿350.00
inventory 250mg
10-20 days ฿860.00
inventory 1g
10-20 days ฿3,400.00

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6-Chloro-1H-indazole-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo functional group transformations, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing new active ingredients w

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to undergo functional group transformations, enabling the formation of complex heterocyclic systems. Commonly employed in the preparation of bioactive molecules targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing new active ingredients with potential pesticidal or fungicidal activity. Its structural features make it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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