183015-90-9

Basic information

• Product Name: [C₆H₅NHC(O)C₆H₄C(O)O]Sb(SCH₂)2
• Synonyms: [C₆H₅NHC(O)C₆H₄C(O)O]Sb(SCH₂)2
• CAS NO: 183015-90-9
• Molecular Weight: 454.174
• Mol File: 183015-90-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [C₆H₅NHC(O)C₆H₄C(O)O]Sb(SCH₂)2(CAS DataBase Reference)
• NIST Chemistry Reference: [C₆H₅NHC(O)C₆H₄C(O)O]Sb(SCH₂)2(183015-90-9)
• EPA Substance Registry System: [C₆H₅NHC(O)C₆H₄C(O)O]Sb(SCH₂)2(183015-90-9)

Safety Data

• Hazardous Substances Data: 183015-90-9(Hazardous Substances Data)

Upstream product

• 4727-29-1 phthalanilic acid 
• 3741-30-8 ethane-1,2-dithiolatoantimony(III) chloride 

Relevant articles and documents

Synthesis and characterization of some antimony(III) derivatives of phthalanilic and maleanilic acids

Some antimony(III) derivatives of phthalanilic and maleanilic acids of the type [L]3Sb and [L]SbSCH2CH2S (where L=phthalanilate and maleanilate anions] have been synthesised by the reactions of antimony trichloride and 2-chloro-1, 3-dithia-2-stibacyclopentane, each, with phthalanilic and maleanilic acids in 1:3 and 1:1 molar ratios respectively in refluxing acetonitrile. Alternatively, these derivatives have also been synthesised by refluxing antimony trichloride and 2-chloro-1, 3-dithia-2-stibacyclopentane, each, with sodium phthalanilate and sodium maleanilate (prepared in situ by the reaction of sodium methoxide with phthalanilic and maleanilic acid in methanol) in 1:3 and 1:1 molar ratios respectively in methanol. These derivatives are characterised by elemental analysis, as well as IR and 1H NMR spectral studies.