Methyl 2-amino-4-methylbenzo[d]thiazole-6-carboxylate

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Reagent Code: #42661
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CAS Number 225525-63-3

science Other reagents with same CAS 225525-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.2600 g/mol
Formula C₁₀H₁₀N₂O₂S
badge Registry Numbers
MDL Number MFCD11695063
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both amino and carboxylate functional groups, makes it a versatile building block for the development of pharmaceuticals, particularly in the synthesis of thiazole-based drugs. It is often employed in the creation of compounds with potential antibacterial, antifungal, or anti-inflammatory properties. Additionally, its application extends to the research and development of novel organic materials, where it contributes to the design of molecules with specific electronic or optical properties.

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100mg
10-20 days ฿2,457.00

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Methyl 2-amino-4-methylbenzo[d]thiazole-6-carboxylate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both amino and carboxylate functional groups, makes it a versatile building block for the development of pharmaceuticals, particularly in the synthesis of thiazole-based drugs. It is often employed in the creation of compounds with potential antibacterial, antifungal, or anti-inflammatory properties. Additionally, its ap

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both amino and carboxylate functional groups, makes it a versatile building block for the development of pharmaceuticals, particularly in the synthesis of thiazole-based drugs. It is often employed in the creation of compounds with potential antibacterial, antifungal, or anti-inflammatory properties. Additionally, its application extends to the research and development of novel organic materials, where it contributes to the design of molecules with specific electronic or optical properties.

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