Thiazole-2-carbonyl chloride

≥95%

Reagent Code: #240198
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CAS Number 30216-57-0

science Other reagents with same CAS 30216-57-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.59 g/mol
Formula C₄H₂ClNOS
badge Registry Numbers
MDL Number MFCD06658970
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its reactive chloride group allows for easy attachment to other molecules, making it valuable in constructing heterocyclic compounds with biological activity. Commonly employed in the preparation of thiazole-based drug candidates and agrochemicals due to its ability to enhance metabolic stability and binding affinity. Also utilized in organic synthesis to introduce the thiazole-2-carbonyl moiety into larger molecules for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,660.00
Thiazole-2-carbonyl chloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its reactive chloride group allows for easy attachment to other molecules, making it valuable in constructing heterocyclic compounds with biological activity. Commonly employed in the preparation of thiazole-based drug candidates and agrochemicals due to its ability to enhance metabolic stability and binding affinity. Also utilized in organic synthesis to introduce the th

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its reactive chloride group allows for easy attachment to other molecules, making it valuable in constructing heterocyclic compounds with biological activity. Commonly employed in the preparation of thiazole-based drug candidates and agrochemicals due to its ability to enhance metabolic stability and binding affinity. Also utilized in organic synthesis to introduce the thiazole-2-carbonyl moiety into larger molecules for structure-activity relationship studies.

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