Methyl 2,3-dimethoxybenzoate

95%

Reagent Code: #206907
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CAS Number 2150-42-7

science Other reagents with same CAS 2150-42-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.2 g/mol
Formula C₁₀H₁₂O₄
thermostat Physical Properties
Melting Point 48-52°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its methoxy-substituted aromatic structure makes it valuable in the development of bioactive molecules, including potential drug candidates targeting central nervous system disorders. It also serves in the synthesis of fragrances and flavoring agents due to its aromatic characteristics. Additionally, it can act as a building block in the formation of more complex esters and benzoyl derivatives through esterification or cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿840.00
inventory 5g
10-20 days ฿2,730.00
inventory 25g
10-20 days ฿4,520.00

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Methyl 2,3-dimethoxybenzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its methoxy-substituted aromatic structure makes it valuable in the development of bioactive molecules, including potential drug candidates targeting central nervous system disorders. It also serves in the synthesis of fragrances and flavoring agents due to its aromatic characteristics. Additionally, it can act as a building block in the formation of more complex esters and benzoyl derivat

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its methoxy-substituted aromatic structure makes it valuable in the development of bioactive molecules, including potential drug candidates targeting central nervous system disorders. It also serves in the synthesis of fragrances and flavoring agents due to its aromatic characteristics. Additionally, it can act as a building block in the formation of more complex esters and benzoyl derivatives through esterification or cross-coupling reactions.

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