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      2,4-Dichloro-3,5-dimethylphenol CAS 133-53-9

      • 2,4-Dichloro-3,5-dimethylphenol CAS 133-53-9...
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      Detailed introduction



      CAS number:133-53-9
      molecular formula:C8H8Cl2O
      molecular weight:191.05
      EINECS number:205-109-9

      English synonyms

      2,4-Dichloro-3,5-xelenol(DCMX);DICHLORO-m-XYLENOL;2,4-Dichloro-3,5-dimethylphenol(DCMX);2,4-Dichloro-3,5-xylenol,2,4-Dichloro-5-hydroxy-m-xylene;2,4-DICHLORO-3,5-DIMETHYLPHENOL;2,4-DICHLORO-3,5-XYLENOL;2,4-DICHLORO-M-XYLENOL;2,4-dichloro-1,3-xylenol

      Related categories

      Aromatic hydrocarbons; phenol; antibacterial and antifungal agents; sterilization and disinfection; pharmaceutical raw materials; organic chemical industry-organic chemical raw materials; chemical raw materials; raw materials; raw materials; benzene; Antibacterial agent; ;Chemical additives;133-53-9;Industrial chemicals;Fine chemical raw materials;Chemical raw materials;Additives

      Introduction

      2,4-dichloro-3,5-dimethylphenol is a phenol derivative with certain acidity, and is mainly used as an intermediate in organic synthesis and medicinal chemistry.

      Melting point91-96°C
      Boiling point273.74°C(roughestimate)
      Density1.2559(roughestimate)
      Refractive index1.5605(estimate)
      Flash point138°C
      Acidity coefficient(pKa)8.30±0.28(Predicted)
      Shapepowder to crystal
      ColorWhite to Light yellow to Light red
      Merck14,3076
      BRN2209273
      InChIKeyIYOLBFFHPZOQGW-UHFFFAOYSA-N
      CAS database133-53-9(CASDataBaseReference)

      ●  2,4-dichloro-3,5-dimethylphenol is a phenol derivative with certain acidity, and is mainly used as an intermediate in organic synthesis and medicinal chemistry.

      ●  In a three-necked flask equipped with a reflux condenser (open to air), add phenol and manganese sulfate catalyst to water, introduce gaseous hydrochloric acid and dissolve into an aqueous solution, immerse the flask in a preheated oil bath, and stir vigorously with a magnetic stirrer Stir, and slowly add H2O2 (30% concentration solution) dropwise with a syringe during the reaction, and let the mixture stand for 1.5 hours, so that the water and the organic layer in the reaction system can be separated into two phases. The organic phase was collected, dried with anhydrous sodium sulfate, and the obtained filtrate was filtered and concentrated under vacuum, and the target product 2,4-dichloro-3,5-di methyl phenol.

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