CAS 131-09-9: 2-Chloroanthraquinone
Formula:C14H7ClO2
InChI:InChI=1S/C14H7ClO2/c15-8-5-6-11-12(7-8)14(17)10-4-2-1-3-9(10)13(11)16/h1-7H
InChI key:InChIKey=FPKCTSIVDAWGFA-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)C=3C1=CC=CC3)=CC=C(Cl)C2
Synonyms:- 2-Chloro-9,10-anthracenedione
- 2-Chloroanthraquinone
- 9,10-Anthracenedione, 2-chloro-
- β-Chloroanthraquinone
- Anthraquinone, 2-chloro-
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Found 6 products.
2-Chloroanthraquinone
CAS:2-ChloroanthraquinoneFormula:C14H7ClO2Purity:99%Color and Shape: tan powderMolecular weight:242.66g/mol2-Chloroanthraquinone
CAS:2-Chloroanthraquinone is a biochemical.Formula:C14H7ClO2Color and Shape:Beige PowderMolecular weight:242.662-Chloroanthraquinone
CAS:Purity:97.0%Color and Shape:Liquid, No data available.Molecular weight:242.660003662109389,10-Anthracenedione, 2-chloro-
CAS:Formula:C14H7ClO2Purity:99%Color and Shape:SolidMolecular weight:242.65722-Chloroanthraquinone
CAS:Formula:C14H7ClO2Purity:>99.0%(GC)Color and Shape:White to Light orange to Yellow powder to crystalMolecular weight:242.662-ChloroanthraqUinone
CAS:2-Chloroanthraquinone is a synthetic biphenyl-2-carboxylic acid that reacts with amines to form peroxides. It is oxidized by photooxidation in polyvinyl chloride, which leads to the formation of chloroamines. 2-Chloroanthraquinone has been used as an intermediate for the production of many other compounds, including ginsenoside rg1, which has been shown to have antiinflammatory effects. The mechanism for the reaction of 2-chloroanthraquinone with amines is still unclear. The functional theory and mechanistic study are two possible explanations for this reaction.Purity:Min. 95%Ref: 3D-FC41585
Discontinued product
