2,3-Dimethoxybenzoyl chloride

95%

Reagent Code: #178202
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CAS Number 7169-06-4

science Other reagents with same CAS 7169-06-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.62 g/mol
Formula C₉H₉ClO₃
badge Registry Numbers
MDL Number MFCD03424705
inventory_2 Storage & Handling
Storage 2-8°C, argon-filled

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and fine chemicals. Its reactivity makes it valuable in forming amide and ester bonds, especially in the development of active pharmaceutical ingredients (APIs). Commonly employed in the preparation of benzodiazepine derivatives and other heterocyclic compounds with biological activity. Also utilized in organic synthesis for introducing the 2,3-dimethoxybenzoyl group, which can act as a protecting group or modify solubility and stability in complex molecules. Preferred in reactions where controlled acylation is required due to its selective reactivity.

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inventory 250mg
10-20 days ฿3,660.00

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2,3-Dimethoxybenzoyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and fine chemicals. Its reactivity makes it valuable in forming amide and ester bonds, especially in the development of active pharmaceutical ingredients (APIs). Commonly employed in the preparation of benzodiazepine derivatives and other heterocyclic compounds with biological activity. Also utilized in organic synthesis for introducing the 2,3-dimethoxybenzoyl group, which can act as a protecting group or modify solubility and stabili

Used primarily as an intermediate in the synthesis of pharmaceuticals and fine chemicals. Its reactivity makes it valuable in forming amide and ester bonds, especially in the development of active pharmaceutical ingredients (APIs). Commonly employed in the preparation of benzodiazepine derivatives and other heterocyclic compounds with biological activity. Also utilized in organic synthesis for introducing the 2,3-dimethoxybenzoyl group, which can act as a protecting group or modify solubility and stability in complex molecules. Preferred in reactions where controlled acylation is required due to its selective reactivity.

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