m-Acetoxy Benzoic Acid

95%

Reagent Code: #137142
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CAS Number 6304-89-8

science Other reagents with same CAS 6304-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.1574 g/mol
Formula C₉H₈O₄
badge Registry Numbers
MDL Number MFCD00016699
thermostat Physical Properties
Melting Point 131-134 °C
Boiling Point 338.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.29 g/cm3
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It plays a role in the preparation of esters and other derivatives used in drug development. Commonly employed in acetylation reactions where selective protection of hydroxyl groups is required. Also utilized in the synthesis of dyes and fragrances due to its aromatic structure and reactivity. Its acetoxy group facilitates controlled release in prodrug formulations. Suitable for research applications involving carboxylic acid modifications and aromatic substitutions.

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inventory 5g
10-20 days ฿3,950.00

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m-Acetoxy Benzoic Acid
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It plays a role in the preparation of esters and other derivatives used in drug development. Commonly employed in acetylation reactions where selective protection of hydroxyl groups is required. Also utilized in the synthesis of dyes and fragrances due to its aromatic structure and reactivity. Its acetoxy group facilitates controlled release in prodrug formulations. Suitable for research ap

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It plays a role in the preparation of esters and other derivatives used in drug development. Commonly employed in acetylation reactions where selective protection of hydroxyl groups is required. Also utilized in the synthesis of dyes and fragrances due to its aromatic structure and reactivity. Its acetoxy group facilitates controlled release in prodrug formulations. Suitable for research applications involving carboxylic acid modifications and aromatic substitutions.

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