Methyl 2-chlorobenzo[d]oxazole-5-carboxylate

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Reagent Code: #83406
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CAS Number 54120-92-2

science Other reagents with same CAS 54120-92-2

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scatter_plot Molecular Information
Weight 211.60 g/mol
Formula C₉H₆ClNO₃
badge Registry Numbers
MDL Number MFCD17019483
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

This chemical, Methyl 2-chlorobenzo[d]oxazole-5-carboxylate, is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure features a fused benzoxazole ring system with a chlorine substituent at the 2-position and a methyl carboxylate ester group at the 5-position, making it a versatile building block for creating molecules with potential biological activity. The 2-chloro group provides a reactive site for nucleophilic substitution, enabling further derivatization. It is often employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery for targeting diseases such as cancer, inflammation, and infections. Additionally, its reactivity allows for further functionalization, enabling the creation of more complex structures for medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿45,000.00
inventory 100mg
10-20 days ฿25,200.00

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Methyl 2-chlorobenzo[d]oxazole-5-carboxylate
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This chemical, Methyl 2-chlorobenzo[d]oxazole-5-carboxylate, is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure features a fused benzoxazole ring system with a chlorine substituent at the 2-position and a methyl carboxylate ester group at the 5-position, making it a versatile building block for creating molecules with potential biological activity. The 2-chloro group provides a reactive site for nucleophilic substitution

This chemical, Methyl 2-chlorobenzo[d]oxazole-5-carboxylate, is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure features a fused benzoxazole ring system with a chlorine substituent at the 2-position and a methyl carboxylate ester group at the 5-position, making it a versatile building block for creating molecules with potential biological activity. The 2-chloro group provides a reactive site for nucleophilic substitution, enabling further derivatization. It is often employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery for targeting diseases such as cancer, inflammation, and infections. Additionally, its reactivity allows for further functionalization, enabling the creation of more complex structures for medicinal chemistry research.

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