ChemicalBook--->CAS DataBase List--->18711-13-2

18711-13-2

18711-13-2 Structure

18711-13-2 Structure
IdentificationMore
[Name]

4,7-DICHLOROISATIN
[CAS]

18711-13-2
[Synonyms]

4,7-DICHLOROINDOLINE-2,3-DIONE
4,7-DICHLOROISATIN
BUTTPARK 50\07-81
4,7-dichloro-1H-indole-2,3-dione
[EINECS(EC#)]

622-637-9
[Molecular Formula]

C8H3Cl2NO2
[MDL Number]

MFCD00047214
[Molecular Weight]

216.02
[MOL File]

18711-13-2.mol
Chemical PropertiesBack Directory
[Appearance]

orange flakes
[Melting point ]

250-252 °C(lit.)
[density ]

1.643±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

8.38±0.20(Predicted)
[color ]

Light yellow to Brown
[BRN ]

168731
[InChI]

InChI=1S/C8H3Cl2NO2/c9-3-1-2-4(10)6-5(3)7(12)8(13)11-6/h1-2H,(H,11,12,13)
[InChIKey]

NUXYYWOWNFEMNH-UHFFFAOYSA-N
[SMILES]

N1C2=C(C(Cl)=CC=C2Cl)C(=O)C1=O
[CAS DataBase Reference]

18711-13-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R36:Irritating to the eyes.
[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
[HS Code ]

29337900
Hazard InformationBack Directory
[Chemical Properties]

orange flakes
[Uses]

Used as an intermediate in organic synthesis.
[Synthesis]

To a mixture of 2,5-Dichloroaniline (1.02 g, 7.84 mmol), anhydrous sodium sulfate (8.94 g, 62.71 mmol), hydroxylamine hydrochloride (2.24 g, 31.35 mmol) and 1M hydrochloric acid (8.0 mL) in water (60 mL) is added chloral hydrate (1.58 g, 9.41 mmol) at room temperature. The resulting mixture is warmed to 55 °C and stirred for 6 hours. While the mixture is cooling to room temperature, solid precipitate is formed and collected by filtration, washed with water and dried under vacuum to yield the hydroxyliminoacetanilide intermediate, which is added in small portions to concentrated sulfuric acid (5.0 mL) that is preheated to 55 °C. The temperature of the reaction mixture is maintained at below 58 °C throughout the addition. After the addition is completed, the dark-colored mixture is heated to 80 °C for 10 minutes before cooling down to room temperature. The mixture is then poured into crushed ice, swirled, and left to stand for 30 minutes. 4,7-Dichloroisatin formed is collected by filtration, washed with water and dried under vacuum.
synthesis of 4,7-Dichloroisatin
Spectrum DetailBack Directory
[Spectrum Detail]

4,7-Dichloroisatin(18711-13-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4,7-Dichloroisatin, 98%(18711-13-2)
[Sigma Aldrich]

18711-13-2(sigmaaldrich)
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