2-(4-bromo-3-methylphenyl)-5-methyl-1,3,4-oxadiazole

95%

Reagent Code: #150831
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CAS Number 148672-44-0

science Other reagents with same CAS 148672-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.10 g/mol
Formula C₁₀H₉BrN₂O
badge Registry Numbers
MDL Number MFCD13192379
thermostat Physical Properties
Boiling Point 349.8±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.465±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports activity in bioactive molecule design, making it valuable in medicinal chemistry research. Also employed in the creation of agrochemicals due to its stability and reactivity in coupling reactions. Commonly utilized in fluorescence-based sensors and optoelectronic materials because of its aromatic and heterocyclic framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,880.00
inventory 250mg
10-20 days ฿17,290.00
inventory 1g
10-20 days ฿34,580.00

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2-(4-bromo-3-methylphenyl)-5-methyl-1,3,4-oxadiazole
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports activity in bioactive molecule design, making it valuable in medicinal chemistry research. Also employed in the creation of agrochemicals due to its stability and reactivity in coupling reactions. Commonly utilized in fluorescence-based sensors and optoelectronic materials because of its aromatic and heterocyclic framework.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports activity in bioactive molecule design, making it valuable in medicinal chemistry research. Also employed in the creation of agrochemicals due to its stability and reactivity in coupling reactions. Commonly utilized in fluorescence-based sensors and optoelectronic materials because of its aromatic and heterocyclic framework.

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