ethyl 3,5-dihydroxy-4-iodobenzoate

95%

Reagent Code: #65042
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CAS Number 692204-84-5

science Other reagents with same CAS 692204-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.07 g/mol
Formula C₉H₉IO₄
badge Registry Numbers
MDL Number MFCD29053057
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both hydroxyl and iodo groups, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is also employed in the creation of specialty chemicals, where its functional groups allow for further chemical modifications, such as cross-coupling reactions or esterification processes. Additionally, it finds use in research settings for studying reaction mechanisms or developing new synthetic methodologies. Its iodine component can be particularly useful in radiolabeling applications for imaging or diagnostic purposes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,421.00
inventory 250mg
10-20 days ฿4,716.00

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ethyl 3,5-dihydroxy-4-iodobenzoate
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both hydroxyl and iodo groups, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is also employed in the creation of specialty chemicals, where its functional groups allow for further chemical modifications, such as cross-coupling reactions or esterification

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both hydroxyl and iodo groups, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is also employed in the creation of specialty chemicals, where its functional groups allow for further chemical modifications, such as cross-coupling reactions or esterification processes. Additionally, it finds use in research settings for studying reaction mechanisms or developing new synthetic methodologies. Its iodine component can be particularly useful in radiolabeling applications for imaging or diagnostic purposes.

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