4-(Thiazol-2-yl)benzaldehyde

98%

Reagent Code: #240749
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CAS Number 198904-53-9

science Other reagents with same CAS 198904-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.23 g/mol
Formula C₁₀H₇NOS
thermostat Physical Properties
Boiling Point 350.3°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. Its structure enables conjugation into larger bioactive molecules, enhancing drug stability and target interaction. Commonly employed in the preparation of fluorescent probes due to its ability to form conjugated Schiff bases, which exhibit strong emission properties useful in bioimaging and sensor technologies. Also utilized in the fabrication of organic semiconductors and optoelectronic materials owing to its electron-accepting and π-conjugated framework.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿385.00
inventory 5g
10-20 days ฿6,680.00
inventory 1g
10-20 days ฿1,790.00
inventory 25g
10-20 days ฿25,710.00

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4-(Thiazol-2-yl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. Its structure enables conjugation into larger bioactive molecules, enhancing drug stability and target interaction. Commonly employed in the preparation of fluorescent probes due to its ability to form conjugated Schiff bases, which exhibit strong emission properties useful in bioimaging and sensor technologies. Also utilized in the fabrication of organic semiconductors a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. Its structure enables conjugation into larger bioactive molecules, enhancing drug stability and target interaction. Commonly employed in the preparation of fluorescent probes due to its ability to form conjugated Schiff bases, which exhibit strong emission properties useful in bioimaging and sensor technologies. Also utilized in the fabrication of organic semiconductors and optoelectronic materials owing to its electron-accepting and π-conjugated framework.

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