5-Methylthiazole-2-carbonitrile

≥95%

Reagent Code: #213765
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CAS Number 100516-71-0

science Other reagents with same CAS 100516-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.16 g/mol
Formula C₅H₄N₂S
badge Registry Numbers
MDL Number MFCD11109818
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and antifungal properties. It serves as a building block in agrochemicals for creating pesticides and herbicides due to its reactive nitrile and heterocyclic structure. Also employed in the preparation of dyes and functional materials where thiazole derivatives enhance stability and electronic properties. Its versatility makes it valuable in research laboratories for designing novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,310.00
inventory 250mg
10-20 days ฿31,820.00
inventory 1g
10-20 days ฿64,340.00

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5-Methylthiazole-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and antifungal properties. It serves as a building block in agrochemicals for creating pesticides and herbicides due to its reactive nitrile and heterocyclic structure. Also employed in the preparation of dyes and functional materials where thiazole derivatives enhance stability and electronic properties. Its versatility makes it valuable in research laboratories for

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and antifungal properties. It serves as a building block in agrochemicals for creating pesticides and herbicides due to its reactive nitrile and heterocyclic structure. Also employed in the preparation of dyes and functional materials where thiazole derivatives enhance stability and electronic properties. Its versatility makes it valuable in research laboratories for designing novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies.

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