2,3-Dimethoxybenzyl Alcohol

99 %

Reagent Code: #170891
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CAS Number 5653-67-8

science Other reagents with same CAS 5653-67-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.19 g/mol
Formula C₉H₁₂O₃
badge Registry Numbers
MDL Number MFCD00004612
thermostat Physical Properties
Melting Point 48-51 °C (Lit.)
Boiling Point 257.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its functional groups make it suitable for derivatization in the development of active pharmaceutical ingredients (APIs). Commonly employed in the synthesis of alkaloids and other biologically active compounds due to the reactivity of the alcohol and ether functionalities. Also utilized in fragrance chemistry, where it contributes to the creation of complex aromatic molecules. Its methoxy-substituted aromatic ring provides stability and influences electronic properties in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,250.00
inventory 25g
10-20 days ฿4,400.00

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2,3-Dimethoxybenzyl Alcohol
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its functional groups make it suitable for derivatization in the development of active pharmaceutical ingredients (APIs). Commonly employed in the synthesis of alkaloids and other biologically active compounds due to the reactivity of the alcohol and ether functionalities. Also utilized in fragrance chemistry, where it contributes to the creation of complex aromatic molecules. Its methoxy-

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its functional groups make it suitable for derivatization in the development of active pharmaceutical ingredients (APIs). Commonly employed in the synthesis of alkaloids and other biologically active compounds due to the reactivity of the alcohol and ether functionalities. Also utilized in fragrance chemistry, where it contributes to the creation of complex aromatic molecules. Its methoxy-substituted aromatic ring provides stability and influences electronic properties in synthetic pathways.

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