2-Ethylthiazole-4-carboxylic acid hydrochloride

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Reagent Code: #183708
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CAS Number 1646152-52-4

science Other reagents with same CAS 1646152-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.65 g/mol
Formula C₆H₈ClNO₂S
badge Registry Numbers
MDL Number MFCD23703031
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antifungal and antibacterial agents. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with biological activity. Also employed in agrochemical research for designing new crop protection agents due to its ability to enhance molecular stability and reactivity. Commonly utilized in laboratory settings for derivatization reactions to study reaction mechanisms or improve compound solubility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,280.00
inventory 250mg
10-20 days ฿4,560.00
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2-Ethylthiazole-4-carboxylic acid hydrochloride
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antifungal and antibacterial agents. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with biological activity. Also employed in agrochemical research for designing new crop protection agents due to its ability to enhance molecular stability and reactivity. Commonly utilized in laboratory settings for derivatization reactions to study reaction mechan

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antifungal and antibacterial agents. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with biological activity. Also employed in agrochemical research for designing new crop protection agents due to its ability to enhance molecular stability and reactivity. Commonly utilized in laboratory settings for derivatization reactions to study reaction mechanisms or improve compound solubility.

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