1-Benzyl-3-(chloromethyl)-1H-indazole

≥97%

Reagent Code: #68096
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CAS Number 131427-22-0

science Other reagents with same CAS 131427-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.73 g/mol
Formula C₁₅H₁₃ClN₂
badge Registry Numbers
MDL Number MFCD20134218
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a chloromethyl group, makes it a versatile building block for the development of potential pharmaceutical agents. It is often employed in the creation of indazole derivatives, which are known for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additionally, it serves as a precursor in the design of enzyme inhibitors and receptor modulators, contributing to drug discovery and development efforts. Its reactivity allows for further functionalization, enabling researchers to explore a wide range of chemical modifications to optimize biological activity and drug efficacy.

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Test Parameter Specification
Appearance White to yellow solid
Purity 97-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,280.00
inventory 1g
10-20 days ฿12,850.00

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1-Benzyl-3-(chloromethyl)-1H-indazole
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a chloromethyl group, makes it a versatile building block for the development of potential pharmaceutical agents. It is often employed in the creation of indazole derivatives, which are known for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additional

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a chloromethyl group, makes it a versatile building block for the development of potential pharmaceutical agents. It is often employed in the creation of indazole derivatives, which are known for their therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additionally, it serves as a precursor in the design of enzyme inhibitors and receptor modulators, contributing to drug discovery and development efforts. Its reactivity allows for further functionalization, enabling researchers to explore a wide range of chemical modifications to optimize biological activity and drug efficacy.

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