2-Hydroxy-3-(methylthio)benzoic acid

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Reagent Code: #196424
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CAS Number 67127-64-4

science Other reagents with same CAS 67127-64-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.21 g/mol
Formula C₈H₈O₃S
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MDL Number MFCD16999038
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfur-containing bioactive compounds. Its structure supports the creation of thioether derivatives with potential antimicrobial or anti-inflammatory properties. Also employed in research for designing novel organic molecules where a methylthio-functionalized aromatic backbone is required. Shows utility in coordination chemistry as a ligand for metal ions due to the presence of carboxylic acid and hydroxyl groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,410.00
inventory 250mg
10-20 days ฿28,900.00
inventory 1g
10-20 days ฿57,800.00

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2-Hydroxy-3-(methylthio)benzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfur-containing bioactive compounds. Its structure supports the creation of thioether derivatives with potential antimicrobial or anti-inflammatory properties. Also employed in research for designing novel organic molecules where a methylthio-functionalized aromatic backbone is required. Shows utility in coordination chemistry as a ligand for metal ions due to the presence of carboxylic aci

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of sulfur-containing bioactive compounds. Its structure supports the creation of thioether derivatives with potential antimicrobial or anti-inflammatory properties. Also employed in research for designing novel organic molecules where a methylthio-functionalized aromatic backbone is required. Shows utility in coordination chemistry as a ligand for metal ions due to the presence of carboxylic acid and hydroxyl groups.

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