(5-Bromopyridin-2-yl)hydrazine

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Reagent Code: #145317
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CAS Number 77992-44-0

science Other reagents with same CAS 77992-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.03 g/mol
Formula C₅H₆BrN₃
badge Registry Numbers
MDL Number MFCD00513424
thermostat Physical Properties
Melting Point 132-137°C
Boiling Point 305.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its structure allows for easy functionalization in heterocyclic chemistry, making it valuable in creating pyrazole, triazole, and other nitrogen-containing ring systems found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine handle enabling cross-coupling reactions. Also utilized in agrochemical research for designing novel active ingredients with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,040.00
inventory 25g
10-20 days ฿2,600.00
inventory 100g
10-20 days ฿10,050.00

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(5-Bromopyridin-2-yl)hydrazine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its structure allows for easy functionalization in heterocyclic chemistry, making it valuable in creating pyrazole, triazole, and other nitrogen-containing ring systems found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine handle enabling cross-coupling reactions. Also utili

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its structure allows for easy functionalization in heterocyclic chemistry, making it valuable in creating pyrazole, triazole, and other nitrogen-containing ring systems found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine handle enabling cross-coupling reactions. Also utilized in agrochemical research for designing novel active ingredients with improved efficacy and selectivity.

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