2-methylthiazole-5-carbaldehyde

95%

Reagent Code: #205529
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CAS Number 1003-60-7

science Other reagents with same CAS 1003-60-7

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Weight 127.17 g/mol
Formula C₅H₅NOS
badge Registry Numbers
MDL Number MFCD09864617
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of thiamine (vitamin B1). It also serves as a building block in the development of agrochemicals and biologically active compounds due to its heterocyclic structure. Its aldehyde functional group allows for easy modification in organic reactions, making it valuable in medicinal chemistry for creating derivatives with potential antimicrobial or antifungal properties. Additionally, it is employed in research settings for the preparation of fluorescent probes and sensors owing to the electron-rich nature of the thiazole ring.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,020.00
inventory 5g
10-20 days ฿4,920.00

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2-methylthiazole-5-carbaldehyde
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Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of thiamine (vitamin B1). It also serves as a building block in the development of agrochemicals and biologically active compounds due to its heterocyclic structure. Its aldehyde functional group allows for easy modification in organic reactions, making it valuable in medicinal chemistry for creating derivatives with potential antimicrobial or antifungal properties. Additionally, it is employed in research setting

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of thiamine (vitamin B1). It also serves as a building block in the development of agrochemicals and biologically active compounds due to its heterocyclic structure. Its aldehyde functional group allows for easy modification in organic reactions, making it valuable in medicinal chemistry for creating derivatives with potential antimicrobial or antifungal properties. Additionally, it is employed in research settings for the preparation of fluorescent probes and sensors owing to the electron-rich nature of the thiazole ring.

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