2-chlorothiazole-4-carbaldehyde

≥95%

Reagent Code: #159213
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CAS Number 5198-79-8

science Other reagents with same CAS 5198-79-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.58 g/mol
Formula C₄H₂ClNOS
badge Registry Numbers
MDL Number MFCD09702023
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other biologically active compounds. It plays an important role in agrochemical manufacturing, serving as a building block for pesticides and herbicides due to its reactive functional groups. Its structure allows for easy modification in organic reactions, making it valuable in research and development of new heterocyclic compounds. Commonly employed in condensation and coupling reactions to form more complex molecules with enhanced biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿750.00
250mg
10-20 days ฿970.00
5g
10-20 days ฿17,360.00
10g
10-20 days ฿34,720.00
1g
10-20 days ฿3,700.00
2-chlorothiazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other biologically active compounds. It plays an important role in agrochemical manufacturing, serving as a building block for pesticides and herbicides due to its reactive functional groups. Its structure allows for easy modification in organic reactions, making it valuable in research and development of new heterocyclic compounds. Commonly employed in condensation and coupling re

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other biologically active compounds. It plays an important role in agrochemical manufacturing, serving as a building block for pesticides and herbicides due to its reactive functional groups. Its structure allows for easy modification in organic reactions, making it valuable in research and development of new heterocyclic compounds. Commonly employed in condensation and coupling reactions to form more complex molecules with enhanced biological activity.

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