4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide

97%

Reagent Code: #204691
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CAS Number 61292-08-8

science Other reagents with same CAS 61292-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.29 g/mol
Formula C₁₁H₁₁N₃OS
badge Registry Numbers
MDL Number MFCD00174004
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceuticals with antimicrobial, antifungal, and anti-inflammatory properties. Its hydrazide functionality allows for easy derivatization to form Schiff bases and other heterocyclic compounds that are often explored in drug discovery. Commonly employed in the development of novel thiazole-based medicinal agents due to its ability to enhance metabolic stability and binding affinity. Also utilized in agrochemical research for designing new pesticides and herbicides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,490.00
4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide
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Used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceuticals with antimicrobial, antifungal, and anti-inflammatory properties. Its hydrazide functionality allows for easy derivatization to form Schiff bases and other heterocyclic compounds that are often explored in drug discovery. Commonly employed in the development of novel thiazole-based medicinal agents due to its ability to enhance metabolic stability and binding affinity. Also utilized in agrochemical researc

Used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceuticals with antimicrobial, antifungal, and anti-inflammatory properties. Its hydrazide functionality allows for easy derivatization to form Schiff bases and other heterocyclic compounds that are often explored in drug discovery. Commonly employed in the development of novel thiazole-based medicinal agents due to its ability to enhance metabolic stability and binding affinity. Also utilized in agrochemical research for designing new pesticides and herbicides with improved efficacy and selectivity.

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