CAS 937-20-2: 2,4′-Dichloroacetophenone
Formula:C8H6Cl2O
InChI:InChI=1S/C8H6Cl2O/c9-5-8(11)6-1-3-7(10)4-2-6/h1-4H,5H2
InChI key:InChIKey=FWDFNLVLIXAOMX-UHFFFAOYSA-N
SMILES:C(CCl)(=O)C1=CC=C(Cl)C=C1
Synonyms:- Ethanone, 2-chloro-1-(4-chlorophenyl)-
- Acetophenone, 2,4′-dichloro-
- α-Chloro-p-chloroacetophenone
- 2-Chloro-1-(4-chlorophenyl)ethanone
- p-Chlorophenacyl chloride
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Found 7 products.
4-Chlorophenacyl Chloride
CAS:Formula:C8H6Cl2OPurity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:189.042-Chloro-1-(4-chlorophenyl)ethanone
CAS:Controlled ProductApplications 2-chloro-1-(4-chlorophenyl)ethanone (cas# 937-20-2) is a useful research chemical.Formula:C8H6OCl2Color and Shape:NeatMolecular weight:189.032-Chloro-1-(4-chlorophenyl)ethanone
CAS:Purity:95.0%Color and Shape:Solid, White - Almost white powderMolecular weight:189.03999328613282-Chloro-1-(4-chlorophenyl)ethanone
CAS:2-Chloro-1-(4-chlorophenyl)ethanone is a pyrazole derivative that inhibits the production of proinflammatory cytokines, such as tumor necrosis factor-α (TNF-α), interleukin 1β (IL-1β), and IL-6. It also exhibits significant anti-inflammatory activity. 2-Chloro-1-(4-chlorophenyl)ethanone is synthesized from the Grignard reagent and chloroacetaldehyde. The synthesis proceeds in two steps: first, the Grignard reagent is added to chloroacetaldehyde in DMF at -78°C to form an organometallic intermediate; second, the organometallic intermediate reacts with an acid chloride to produce the desired product. This reaction can be catalyzed by aluminium chloride or zinc chloride. 2CPAE has a high solubility in organic solvents and surfactants such as sodium dodecylFormula:C8H6Cl2OPurity:Min. 95%Molecular weight:189.04 g/mol2-Chloro-1-(4-chlorophenyl)ethanone
CAS:Formula:C8H6Cl2OPurity:97%Color and Shape:SolidMolecular weight:189.0386
