2-Chloroethyl ethyl ether

• Category :

  Intermediates/Pharmaceutical intermediates

• Synonyms :

  1-Chloro-2-ethoxyethane;2-Chloroethyl ether;2-Ethoxyethylchloride;

• CAS NO :

  628-34-2

• EC NO :

  211-037-9

• Molecular Formula :

  C₄H₉ClO

• Molecular Weight :

  108.57

• Main Specifications :

  99% min

• InChI :

  InChI=1/C4H9ClO/c1-2-6-4-3-5/h2-4H2,1H3

• Packing :

  25kg，50kg 200kg

• Product description :

  What is the chemical of 2-Chloroethyl ethyl ether ? Appearance: Colorless to pale yellow transparent liquid ; Assay：99%min by GC ; IR Identity: conform to standard ; HNMR： conform to standard ; carbon spectrum: conform to standard ; Water by K. F.:0.5% max or as per the customer’s request ; Loss on drying:0.5% max. or as per the customer’s request ; Melting point: -60 °C; boiling point: 107–108°C; ============================================================================= This compound is mainly used as an organic synthesis intermediate and is widely applied in the fields of chemical engineering and pharmaceuticals. Specific uses include: Used for synthesizing drugs, pesticides, and other fine chemicals. As an important chemical raw material, it participates in various organic reactions, such as when reacting with Grignard reagents, chlorine atoms can be replaced by alkyl groups. three Used in laboratory and industrial production for the preparation of ethers, alcohols, and other functional molecules. In addition, 628-34-2 is classified as a flammable and toxic chemical and should be sealed and stored in a cool, dry, well ventilated flammable area, away from oxidants and acidic substances ============================================================================ Main synthesis route: The synthesis of 2-chloroethyl ether usually starts with ethylene glycol monoethyl ether (2-ethylethoxyethanol, CAS number: 110-80-5) as the starting material, and is obtained by reacting with chlorination reagents such as sulfonyl chloride, phosphorus trichloride, or hydrochloric acid. This route is relatively mature in industry and the reaction conditions are relatively mild. twelve Other possible routes: Other synthetic pathways have also been reported in the literature, such as the Williamson ether synthesis reaction between chloroethanol and sodium ethoxide, or the chlorination reaction starting from ethylene oxide and reacting with ethanol

• Uses :

  as an organic synthesis intermediate

• Molecular Structure :