2,4-Dihydroxy-3-methoxybenzaldehyde

95%

Reagent Code: #177371
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CAS Number 58922-29-5

science Other reagents with same CAS 58922-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.15 g/mol
Formula C₈H₈O₄
badge Registry Numbers
MDL Number MFCD19301266
thermostat Physical Properties
Melting Point 85.5-86.5 °C
Boiling Point 130-140 °C(Press: 1 Torr)
inventory_2 Storage & Handling
Density 1.378±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the preparation of bioactive compounds due to the presence of multiple functional groups (aldehyde and phenolic hydroxyls). Its structure supports condensation reactions, making it useful in the development of Schiff bases and other derivatives with potential antimicrobial or antioxidant properties. Also employed in research for synthesizing natural product analogs and in the study of reaction mechanisms involving polyhydroxy aromatic aldehydes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,250.00
inventory 250mg
10-20 days ฿18,810.00
inventory 1g
10-20 days ฿41,370.00

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2,4-Dihydroxy-3-methoxybenzaldehyde
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the preparation of bioactive compounds due to the presence of multiple functional groups (aldehyde and phenolic hydroxyls). Its structure supports condensation reactions, making it useful in the development of Schiff bases and other derivatives with potential antimicrobial or antioxidant properties. Also employed in research for synthesizing natural product analogs and in the study of reacti

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the preparation of bioactive compounds due to the presence of multiple functional groups (aldehyde and phenolic hydroxyls). Its structure supports condensation reactions, making it useful in the development of Schiff bases and other derivatives with potential antimicrobial or antioxidant properties. Also employed in research for synthesizing natural product analogs and in the study of reaction mechanisms involving polyhydroxy aromatic aldehydes.

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