4-Methylphenylglyoxal hydrate

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Reagent Code: #207584
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CAS Number 16208-14-3

science Other reagents with same CAS 16208-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.18 g/mol
Formula C₉H₁₀O₃
badge Registry Numbers
MDL Number MFCD00234532
thermostat Physical Properties
Boiling Point 289.1°C
inventory_2 Storage & Handling
Density 1.252g/mL
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds, including imidazoles and pyrazines, which are common structures in bioactive molecules. Its reactivity allows for selective transformations in multi-step syntheses, making it valuable in drug development and medicinal chemistry research. Additionally, it finds use in the study of glycation reactions due to its structural similarity to reactive carbonyl species involved in metabolic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿720.00
inventory 250mg
10-20 days ฿1,650.00
inventory 1g
10-20 days ฿4,080.00
inventory 5g
10-20 days ฿11,270.00
inventory 25g
10-20 days ฿25,880.00

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4-Methylphenylglyoxal hydrate
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Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds, including imidazoles and pyrazines, which are common structures in bioactive molecules. Its reactivity allows for selective transformations in multi-step syntheses, making it valuable in drug development and medicinal chemistry research. Additionally, it finds use in the study of glycation reactions due to

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds, including imidazoles and pyrazines, which are common structures in bioactive molecules. Its reactivity allows for selective transformations in multi-step syntheses, making it valuable in drug development and medicinal chemistry research. Additionally, it finds use in the study of glycation reactions due to its structural similarity to reactive carbonyl species involved in metabolic pathways.

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