6-Chloro-1H-indazole-4-carboxylic acid

≥95%

Reagent Code: #162123
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CAS Number 885522-12-3

science Other reagents with same CAS 885522-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.59 g/mol
Formula C₈H₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD07781757
inventory_2 Storage & Handling
Storage Room temperature, dry seal

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 ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in research settings for designing drugs that modulate signaling pathways involved in inflammation and tumor growth. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies to optimize drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,250.00
inventory 1g
10-20 days ฿14,200.00
inventory 100mg
10-20 days ฿3,150.00

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6-Chloro-1H-indazole-4-carboxylic acid
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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 ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in research settings for designing drugs that modulate signaling pathways involved in inflammation and tumor growth. Also utilized in the preparation of analogs for structure-activity relationship
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 ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in research settings for designing drugs that modulate signaling pathways involved in inflammation and tumor growth. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies to optimize drug potency and selectivity.
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