3-(4-Bromophenyl)-1-methyl-1H-1,2,4-triazole

95%

Reagent Code: #149191
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CAS Number 1184174-04-6

science Other reagents with same CAS 1184174-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.08 g/mol
Formula C₉H₈BrN₃
badge Registry Numbers
MDL Number MFCD16987729
thermostat Physical Properties
Boiling Point 361.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Dry, room temperature

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of antifungal and anticancer agents. Its structure supports activity against certain enzyme targets, making it valuable in medicinal chemistry for designing new drug candidates. Also employed in agrochemical research for creating novel pesticides with improved efficacy. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to the bromine moiety, which allows further functionalization through cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,820.00
inventory 1g
10-20 days ฿37,770.00

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3-(4-Bromophenyl)-1-methyl-1H-1,2,4-triazole
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Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of antifungal and anticancer agents. Its structure supports activity against certain enzyme targets, making it valuable in medicinal chemistry for designing new drug candidates. Also employed in agrochemical research for creating novel pesticides with improved efficacy. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to the bromine moiety,

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of antifungal and anticancer agents. Its structure supports activity against certain enzyme targets, making it valuable in medicinal chemistry for designing new drug candidates. Also employed in agrochemical research for creating novel pesticides with improved efficacy. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to the bromine moiety, which allows further functionalization through cross-coupling reactions.

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