(4-Methyl-1,3-thiazol-2-yl)methanamine

98%

Reagent Code: #213884
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CAS Number 51221-45-5

science Other reagents with same CAS 51221-45-5

blur_circular Chemical Specifications

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Weight 128.2 g/mol
Formula C₅H₈N₂S
inventory_2 Storage & Handling
Storage 2-8°C

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Used in pharmaceutical synthesis as a building block for heterocyclic compounds, particularly in the development of bioactive molecules and drug candidates. Its amine and thiazole functionalities make it valuable for forming amide bonds or participating in condensation reactions to create more complex structures. Commonly applied in research settings for designing kinase inhibitors, antimicrobial agents, and anti-inflammatory compounds. Also utilized in agrochemical research for developing novel pesticides and herbicides due to the thiazole ring’s metabolic stability and favorable electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,100.00

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(4-Methyl-1,3-thiazol-2-yl)methanamine
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Used in pharmaceutical synthesis as a building block for heterocyclic compounds, particularly in the development of bioactive molecules and drug candidates. Its amine and thiazole functionalities make it valuable for forming amide bonds or participating in condensation reactions to create more complex structures. Commonly applied in research settings for designing kinase inhibitors, antimicrobial agents, and anti-inflammatory compounds. Also utilized in agrochemical research for developing novel pesticid

Used in pharmaceutical synthesis as a building block for heterocyclic compounds, particularly in the development of bioactive molecules and drug candidates. Its amine and thiazole functionalities make it valuable for forming amide bonds or participating in condensation reactions to create more complex structures. Commonly applied in research settings for designing kinase inhibitors, antimicrobial agents, and anti-inflammatory compounds. Also utilized in agrochemical research for developing novel pesticides and herbicides due to the thiazole ring’s metabolic stability and favorable electronic properties.

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