| Identification | More |  [Name]
  5-Chloroisatin |  [CAS]
  17630-76-1 |  [Synonyms]
  5-CHLOR-2,3-DIOXOINDOLIN 5-CHLOR-2,3-INDOLINDION 5-CHLORO-1H-INDOLE-2,3-DIONE 5-CHLORO-2,3-INDOLINEDIONE 5-CHLOROINDOLE-2,3-DIONE 5-CHLOROISATIN AKOS BBS-00000996 AURORA KA-5424 BUTTPARK 50\07-91 TIMTEC-BB SBB003741 1H-Indole-2,3-dione,5-chloro- 5-choroisatin 5-Chlorisatin 5-CHLORISATIDE 5-CHLOROISATIN/5-CHLORO-2,3-INDOLINEDIONE 5-Chloroindolin-2,3-dione 5-Chloroisatin  ,98% |  [EINECS(EC#)]
  241-614-0 |  [Molecular Formula]
  C8H4ClNO2 |  [MDL Number]
  MFCD00014567 |  [Molecular Weight]
  181.58 |  [MOL File]
  17630-76-1.mol |  
 | Chemical Properties | Back Directory |  [Appearance]
  pale yellow to reddish or yellow-brownish powder |  [Melting point ]
  254-258 °C (lit.) |  [density ]
  1.3743 (rough estimate) |  [refractive index ]
  1.5560 (estimate) |  [storage temp. ]
  Sealed in dry,Room Temperature |  [form ]
  Powder |  [pka]
  8.65±0.20(Predicted) |  [Water Solubility ]
  insoluble |  [Detection Methods]
  HPLC,NMR |  [BRN ]
  383759 |  [InChI]
  InChI=1S/C8H4ClNO2/c9-4-1-2-6-5(3-4)7(11)8(12)10-6/h1-3H,(H,10,11,12) |  [InChIKey]
  XHDJYQWGFIBCEP-UHFFFAOYSA-N |  [SMILES]
  N1C2=C(C=C(Cl)C=C2)C(=O)C1=O |  [CAS DataBase Reference]
  17630-76-1(CAS DataBase Reference) |  
 | Safety Data | Back Directory |  [Hazard Codes ]
  Xi |  [Risk Statements ]
  R36/37/38:Irritating to eyes, respiratory system and skin . |  [Safety Statements ]
  S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . |  [WGK Germany ]
  3 
 |  [Hazard Note ]
  Irritant |  [HS Code ]
  29339900 |  
 | Hazard Information | Back Directory |  [Chemical Properties]
  pale yellow to reddish or yellow-brownish powder |  [Uses]
  5-Chloroisatin is a reagent used in the synthesis of Schiff bases through the reaction with 2-methyl-4-nitroaniline or 4-amino-4,5-dihydro-1H-1,2,3-triazole-5-one. |  [Definition]
  ChEBI: 5-Chloro-1H-indole-2,3-dione is a member of indoles. It has a role as an anticoronaviral agent. |  [General Description]
 
 5-Chloroisatin reacts with substituted 4-amino-4,5-dihydro-1H-1,2,4-triazole-5-ones to yield Schiff bases.  |  
  
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