2-(Pyridin-4-yl)thiazole-5-carbaldehyde

98%

Reagent Code: #96649
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CAS Number 21346-36-1

science Other reagents with same CAS 21346-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.22 g/mol
Formula C₉H₆N₂OS
badge Registry Numbers
MDL Number MFCD11846891
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a pyridine and a thiazole ring, makes it particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the creation of novel drug candidates, especially in the development of compounds targeting neurological disorders and infectious diseases. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives that can exhibit diverse biological properties. Beyond pharmaceutical applications, it is also investigated in material science for the design of organic semiconductors and light-emitting materials due to its conjugated system and electron-rich nature.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,040.00
inventory 100mg
10-20 days ฿11,160.00

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2-(Pyridin-4-yl)thiazole-5-carbaldehyde
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a pyridine and a thiazole ring, makes it particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the creation of novel drug candidates, especially in the development of compounds targeting neurological di

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex molecules. Its structure, featuring both a pyridine and a thiazole ring, makes it particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers frequently employ it in the creation of novel drug candidates, especially in the development of compounds targeting neurological disorders and infectious diseases. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the formation of Schiff bases, hydrazones, and other derivatives that can exhibit diverse biological properties. Beyond pharmaceutical applications, it is also investigated in material science for the design of organic semiconductors and light-emitting materials due to its conjugated system and electron-rich nature.

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