4-(3-Methoxyphenyl)oxazole

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Reagent Code: #213606
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CAS Number 1072880-82-0

science Other reagents with same CAS 1072880-82-0

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Weight 175.18 g/mol
Formula C₁₀H₉NO₂
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MDL Number MFCD11845056
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Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of central nervous system agents. Shows potential in the design of serotonin receptor modulators due to structural similarity to known neuroactive molecules. Also employed in agrochemical research for developing new fungicides and plant growth regulators. Its aromatic and heterocyclic framework makes it valuable in materials science for constructing organic semiconductors and fluorescent dyes. Commonly used in medicinal chemistry for scaffold modification to enhance metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,830.00
inventory 1g
10-20 days ฿23,940.00
inventory 250mg
10-20 days ฿11,380.00

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4-(3-Methoxyphenyl)oxazole
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Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of central nervous system agents. Shows potential in the design of serotonin receptor modulators due to structural similarity to known neuroactive molecules. Also employed in agrochemical research for developing new fungicides and plant growth regulators. Its aromatic and heterocyclic framework makes it valuable in materials science for constructing organic semiconductors and fluoresce

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of central nervous system agents. Shows potential in the design of serotonin receptor modulators due to structural similarity to known neuroactive molecules. Also employed in agrochemical research for developing new fungicides and plant growth regulators. Its aromatic and heterocyclic framework makes it valuable in materials science for constructing organic semiconductors and fluorescent dyes. Commonly used in medicinal chemistry for scaffold modification to enhance metabolic stability and binding affinity.

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